Subscribe to RSS
DOI: 10.1055/s-0042-1751582
1,2-trans-Diaminocyclohexane (DACH) in Asymmetric Catalysis: Nearing Fifty Years of Faithful Service and Counting
Abstract
This review highlights the use of DACH as a versatile ligand in catalytic asymmetric transformations providing mechanistic rationales and relevant comments presented in chronological order for each of the 21 reaction types with references up to December 25, 2023. Intended to be as practically comprehensive as possible, this review assembles useful examples of using DACH as a ligand in organocatalytic or as metal complexes in asymmetric transformations. The resulting enantiomerically enriched, if not pure, chiral non-racemic small molecules are of great utility as value added intermediates in the total synthesis of natural products, in the design and synthesis of medicinally important compounds, and in other areas in organic and bioorganic chemistry where chirality plays a role. The graphic image depicts Spartacus with his arms folded in the same sense of chirality as (R,R)-DACH.
1 Introduction
2 DACH: A Brief Historical Narrative
3 Catalytic Asymmetric Hydrogenation of Alkenes
4 Catalytic Asymmetric Dihydroxylation of Alkenes
5 Catalytic Asymmetric Sulfoxidation and Sulfimidation
6 Catalytic Asymmetric 1,4-Conjugate Addition
6.1 Using Jacobsen’s DACH Metal–salen Complexes as Catalysts
6.2 Using Takemoto’s Bifunctional H-Bonding DACH Thiourea Organocatalyst
6.3 Using DACH Ni(II) Complexes as Catalysts
6.4 Using DACH H-Bonding Catalysis
7 Catalytic Asymmetric Epoxidation of Alkenes
8 Catalytic Asymmetric Claisen Rearrangement
9 Catalytic Asymmetric 1,2-Nucleophilic Addition to Carbonyl Compounds
9.1 Catalytic Asymmetric Addition of Dialkylzinc to Aldehydes and Ketones
9.2 Catalytic Asymmetric Alkynylation of Aldehydes and Ketones
9.3 Catalytic Asymmetric Addition of Cyanide to Aldehydes and Ketones
10 Catalytic Asymmetric Allylic Alkylation
11 Catalytic Asymmetric Cyclopropanation of Alkenes
12 Catalytic Asymmetric Cycloaddition Reactions
13 Catalytic Asymmetric Aziridination of Alkenes
14 Catalytic Asymmetric Hydrogenation of Prochiral Ketones and Imines
15 Catalytic Asymmetric Aldol Reactions
16 Catalytic Asymmetric Opening of Small Ring Systems
16.1 Desymmetrization of meso-Epoxides and meso-Aziridines
16.2 Kinetic Resolution of Racemic Epoxides
16.3 Enantioselective Addition of CO2 to Epoxides
16.4 Enantioselective Ring Opening of Oxetanes
17 Catalytic Asymmetric Strecker Reactions
18 Catalytic Asymmetric Mannich Reactions
19 Catalytic Asymmetric Henry and Aza-Henry Reactions
20 Catalytic Asymmetric Morita–Baylis–Hillman and Rauhut–Currier Reactions
21 Catalytic Asymmetric Petasis Reactions
22 Organocatalytic Asymmetric Cascade Reactions
23 Miscellaneous Catalytic Reactions
24 Conclusion and Outlook
25 DACH Catalysts and Ligands List
Key words
H-bonding catalysis - metal-coordinated catalysis - chiral ligand - enantioselective synthesis - C 2-symmetryPublication History
Received: 01 February 2024
Accepted after revision: 20 March 2024
Article published online:
20 June 2024
© 2024. Thieme. All rights reserved
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Comprehensive Asymmetric Catalysis, Vol. I–III. Pfaltz A, Yamamoto H, Jacobsen EN. Springer; Heidelberg: 1999
- 2 Asymmetric Catalysis on Industrial Scale: Challenges, Approaches, and Solutions, 2nd ed. Blaser HU, Federsel H.-J. Wiley-VCH; Weinheim: 2010
- 3 Applications of Transition Metal Catalysis in Drug Discovery and Development: An Industrial Perspective. Crawley ML, Trost BM. John Wiley & Sons; Hoboken: 2012
- 4 Hartwig JF. Organotransition Metal Chemistry: From Bonding to Catalysis . University Science Books; Melville NY: 2010
- 5 Chakraborty P, Mandal R, Garg N, Sundararaju B. Coord. Chem. Rev. 2021; 444: 214065
- 6 Fanourakis A, Docherty PJ, Chuentragool P, Phipps RJ. ACS Catal. 2020; 10: 10672
- 7 Catalytic Asymmetric Synthesis, 3rd ed. Ojima I. John Wiley & Sons; Hoboken: 2010
- 8 Reyes E, Prieto L, Milelli A. Molecules 2022; 28: 271
- 9 Aukland MH, List B. Pure Appl. Chem. 2021; 93: 1371
- 10 Chen Z, Yang Q.-Q, Du W, Chen Y.-C. Tetrahedron Chem 2022; 2: 100017
- 11 Asymmetric Organocatalysis . In Topics in Current Chemistry, Vol. 291. List B. Springer; Heidelberg: 2009
- 12 MacMillan DW. C. Nature 2008; 455: 304
- 13 Mukherjee S, Yang JW, Hoffmann S, List B. Chem. Rev. 2007; 107: 5471
- 14 Erkkilä A, Majander I, Pihko PM. Chem. Rev. 2007; 107: 5416
- 15 Hayashi Y. Catalytic Asymmetric Synthesis, 4th ed. Akiyama T, Ojima I. John Wiley & Sons; Hoboken: 2022
- 16 Parella R, Jakkampudi S, Zhao JC. G. ChemistrySelect 2021; 6: 2252
- 17 Wang Z. Molecules 2019; 24: 3412
- 18 Fang X, Wang CJ. Chem. Commun. 2014; 51: 1185
- 19 Seyden-Penne J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis. Wiley-VCH; New York: 1995
- 20 Asperger RG, Liu FC. Inorg. Chem. 1965; 4: 1492
- 21 Swift G, Swern D. J. Org. Chem. 1967; 32: 511
- 22 Galsbøl F, Steenbøl P, Sørensen BS, Swahn C.-G, Pilotti Å. Acta Chem. Scand. 1972; 26: 3605
- 23 Larrow JF, Jacobsen EN, Gao Y, Hong Y, Nie X, Zepp CM. J. Org. Chem. 1994; 59: 1939
- 24 Larrow JF, Jacobsen EN. Org. Synth. 1998; 75: 1
- 25 Walsh PJ, Smith DK, Castello C. J. Chem. Educ. 1998; 75: 1459
- 26 Alcindor T, Beauger N. Curr. Oncol. 2011; 18: 18
- 27 Bennani YL, Hanessian S. Chem. Rev. 1997; 97: 3161
- 28 Lucet D, Le-Gall T, Mioskowski C. Angew. Chem. Int. Ed. 1998; 37: 2580
- 29 Kouklovsky C, Langlois Y, Aguilar E, Fernández-García JM, Sikervar V. In Encyclopedia of Reagents for Organic Synthesis . John Wiley & Sons; Chichester: 2014: 1
- 30 McGarrigle EM, Gilheany DG. Chem. Rev. 2005; 105: 1563
- 31 Taylor MS, Jacobsen EN. Angew. Chem. Int. Ed. 2006; 45: 1520
- 32 Doyle AG, Jacobsen EN. Chem. Rev. 2007; 107: 5713
- 33 Connon SJ. Chem. Eur. J. 2006; 12: 5418
- 34 Kizirian JC. Chem. Rev. 2008; 108: 140
- 35 Takemoto Y. Chem. Pharm. Bull. 2010; 58: 593
- 36 Alfonso I. Curr. Org. Synth. 2010; 7: 1
- 37 Zlotin SG, Kochetkov SV. Russ. Chem. Rev. 2015; 84: 1077
- 38 Serdyuk OV, Heckel CM, Tsogoeva SB. Org. Biomol. Chem. 2013; 11: 7051
- 39 Shaw S, White JD. Chem. Rev. 2019; 119: 9381
- 40 Hanaki K, Kashiwabara K, Fujita J. Chem. Lett. 1978; 7: 489
- 41 Knowles WS. Acc. Chem. Res. 1983; 16: 106
- 42 Knowles WS. Angew. Chem. Int. Ed. 2002; 41: 1998
- 43 Hanessian S, Delorme D, Beaudoin S, Leblanc Y. J. Am. Chem. Soc. 1984; 106: 5754
- 44 Focken T, Hanessian S. Beilstein J. Org. Chem. 2014; 10: 1848
- 45 Zassinovich G, Mestroni G, Giadiali S. Chem. Rev. 1992; 92: 1051
- 46 Guo H, Ding K, Dai L. Chin. Sci. Bull. 2004; 49: 2003
- 47 Knowles WS, Noyori R. Acc. Chem. Res. 2007; 40: 1238
- 48 Wen J, Wang F, Zhang X. Chem. Soc. Rev. 2021; 50: 3211
- 49 Fiorini M, Giongo GM. J. Mol. Catal. 1979; 5: 303
- 50 Onuma K, Ito T, Nakamura A. Tetrahedron Lett. 1979; 20: 3163
- 51 Onuma K, Ito T, Nakamura A. Chem. Lett. 1980; 9: 481
- 52 Onuma K, Ito T, Nakamura A. Bull. Chem. Soc. Jpn. 1980; 53: 2012
- 53 Onuma K, Ito T, Nakamura A. Bull. Chem. Soc. Jpn. 1980; 53: 2016
- 54 Zhao B, Wang Z, Ding K. Adv. Synth. Catal. 2006; 348: 1049
- 55 Martin NJ. A, Ozores L, List B. J. Am. Chem. Soc. 2007; 129: 8976
- 56 Frank DJ, Guiet L, Käslin A, Murphy E, Thomas SP. RSC Adv. 2013; 3: 25698
- 57 Arribas I, Álvarez E, Pizzano A. Organometallics 2013; 32: 2497
- 58 Kolb HC, VanNieuwenhze MS, Sharpless KB. Chem. Rev. 1994; 94: 2483
- 59 Zaitsev AB, Adolfsson H. Synthesis 2006; 1725
- 60 Ottenbacher RV, Talsi EP, Bryliakov KP. Russ. Chem. Rev. 2019; 88: 1094
- 61 Hentges SG, Sharpless KB. J. Am. Chem. Soc. 1980; 102: 4263
- 62 Jacobsen EN, Markó I, Mungall WS, Schröder G, Sharpless KB. J. Am. Chem. Soc. 1988; 110: 1968
- 63 Sharpless KB, Amberg W, Bennani YL, Crispino GA, Hartung J, Jeong KS, Kwong HL, Morikawa K, Wang ZM, Xu D, Zhang XL. J. Org. Chem. 1992; 57: 2768
- 64 Norrby PO, Becker H, Sharpless KB. J. Am. Chem. Soc. 1996; 118: 35
- 65 Corey EJ, Noe MC, Grogan MJ. Tetrahedron Lett. 1996; 37: 4899
- 66 Tokles M, Snyder JK. Tetrahedron Lett. 1986; 27: 3951
- 67 Hanessian S, Meffre P, Girard M, Beaudoin S, Sancéau JY, Bennani Y. J. Org. Chem. 1993; 58: 1991
- 68 Costas M, Tipton AK, Chen K, Jo D.-H, Que L. J. Am. Chem. Soc. 2001; 123: 6722
- 69 Costas M, Que LJr. Angew. Chem. Int. Ed. 2002; 41: 2179
- 70 Oldenburg PD, Que LJr. Catal. Today 2006; 117: 15
- 71 Suzuki K, Oldenburg PD, Que LJr. Angew. Chem. Int. Ed. 2008; 47: 1887
- 72 Chow TW.-S, Liu Y, Che C.-M. Chem. Commun. 2011; 47: 11204
- 73 Zang C, Liu Y, Xu Z.-J, Tse C.-W, Guan X, Wei J, Huang J.-S, Che C.-M. Angew. Chem. Int. Ed. 2016; 55: 10253
- 74 Lyakin OY, Bryliakov KP, Talsi EP. Coord. Chem. Rev. 2019; 384: 126
- 75 Yang MM, Wang S, Dong ZB. Synthesis 2022; 54: 5168
- 76 Jia T, Wang M, Liao J. Top. Curr. Chem. 2019; 377: 1
- 77 Trost BM, Rao M. Angew. Chem. Int. Ed. 2015; 54: 5026
- 78 Pitchen P, Dunach E, Deshmukh MN, Kagan HB. J. Am. Chem. Soc. 1984; 106: 8188
- 79 Srour H, Le-Maux P, Chevance S, Simonneaux G. Coord. Chem. Rev. 2013; 257: 3030
- 80 Bryliakov KP. Chem. Rev. 2017; 117: 11406
- 81 Di-Furia F, Modena G, Seraglia R. Synthesis 1984; 325
- 82 Nakajima K, Kojima M, Fujita J. Chem. Lett. 1986; 15: 1483
- 83 Palucki M, Hanson P, Jacobsen EN. Tetrahedron Lett. 1992; 33: 7111
- 84 Saito B, Katsuki T. Tetrahedron Lett. 2001; 42: 8333
- 85 Xuan W, Ye C, Zhang M, Chen Z, Cui Y. Chem. Sci. 2013; 4: 3154
- 86 Zhu C, Chen X, Yang Z, Du X, Liu Y, Cui Y. Chem. Commun. 2013; 49: 7120
- 87 Bryliakov KP. Mini-Rev. Org. Chem. 2012; 11: 87
- 88 Chen Y, Tan R, Zhang Y, Zhao G, Yin D. ChemCatChem 2015; 7: 4066
- 89 Talsi EP, Rybalova TV, Bryliakov KP. ACS Catal. 2015; 5: 4673
- 90 Tanaka H, Nishikawa H, Uchida T, Katsuki T. J. Am. Chem. Soc. 2010; 132: 12034
- 91 Saito B, Katsuki T. Tetrahedron Lett. 2001; 42: 3873
- 92 Inoue M, Shinohara N, Tanabe S, Takahashi T, Okura K, Itoh H, Mizoguchi Y, Iida M, Lee N, Matsuoka S. Nat. Chem. 2010; 2: 280
- 93 Choi J.-Y, Hwang G.-S, Senapati B.-K, Ryu D.-H. Bull. Korean Chem. Soc. 2008; 29: 1879
- 94 Bryliakov KP, Talsi EP. Chem. Eur. J. 2007; 13: 8045
- 95 Cram DJ, Day J, Rayner DR, von-Schriltz DM, Duchamp DJ, Garwood DC. J. Am. Chem. Soc. 1970; 92: 7369
- 96 Annunziata R, Cinquini M, Colonna S, Cozzi F. J. Chem. Soc., Perkin Trans. 1 1981; 3118
- 97 Nishikori H, Ohta C, Oberlin E, Irie R, Katsuki T. Tetrahedron 1999; 55: 13937
- 98 Ohta C, Katsuki T. Tetrahedron Lett. 2001; 42: 3885
- 99 Murakami M, Uchida T, Katsuki T. Tetrahedron Lett. 2001; 42: 7071
- 100 Murakami M, Uchida T, Saito B, Katsuki T. Chirality 2003; 15: 116
- 101 Tamura Y, Uchida T, Katsuki T. Tetrahedron Lett. 2003; 44: 3301
- 102 Uchida T, Tamura Y, Ohba M, Katsuki T. Tetrahedron Lett. 2003; 44: 7965
- 103 Fujita H, Uchida T, Irie R, Katsuki T. Chem. Lett. 2007; 36: 1092
- 104 Perlmutter P. Conjugate Addition Reactions in Organic Synthesis . Tetrahedron Organic Chemistry Series Volume 9. Pergamon; Oxford: 1992
- 105 Byrd KM. Beilstein J. Org. Chem. 2015; 11: 530
- 106 Wynberg H, Helder R. Tetrahedron Lett. 1975; 16: 4057
- 107 Bowmaker A, Clark GR, Seadon JK, Griffith EH, Hunt GW, Amma EL. Angew. Chem. Int. Ed. Engl. 1984; 23: 312
- 108 Schmid TE, Drissi-Amraoui S, Crévisy C, Baslé O, Mauduit M. Beilstein J. Org. Chem. 2015; 11: 2418
- 109 Hayashi M, Matsubara R. Tetrahedron Lett. 2017; 58: 1793
- 110 Zheng K, Liu X, Feng X. Chem. Rev. 2018; 118: 7586
- 111 Myers JK, Jacobsen EN. J. Am. Chem. Soc. 1999; 121: 8959
- 112 Sammis GM, Jacobsen EN. J. Am. Chem. Soc. 2003; 125: 4442
- 113 Gandelman M, Jacobsen EN. Angew. Chem. Int. Ed. 2005; 44: 2393
- 114 Mazet C, Jacobsen EN. Angew. Chem. Int. Ed. 2008; 47: 1762
- 115 Madhavan N, Weck M. Adv. Synth. Catal. 2008; 350: 419
- 116 Madhavan N, Takatani T, Sherrill CD, Weck M. Chem. Eur. J. 2009; 15: 1186
- 117 Lin L, Yin W, Fu X, Zhang J, Ma X, Wang R. Org. Biomol. Chem. 2012; 10: 83
- 118 North M, Watson JM. ChemCatChem 2013; 5: 2405
- 119 Jakhar A, Sadhukhan A, Khan NU. H, Saravanan S, Kureshy RI, Abdi SH. R, Bajaj HC. ChemCatChem 2014; 6: 2656
- 120 Schmid J, Frey W, Peters R. Organometallics 2017; 36: 4313
- 121 Takemoto Y, Miyabe H. Chimia 2007; 61: 269
- 122 Okino T, Hoashi Y, Takemoto Y. J. Am. Chem. Soc. 2003; 125: 12672
- 123 Okino T, Hoashi Y, Furukawa T, Xu X, Takemoto Y. J. Am. Chem. Soc. 2005; 127: 119
- 124 Zhou WM, Liu H, Du DM. Org. Lett. 2008; 10: 2817
- 125 Baslé O, Raimondi W, Duque MD. M. S, Bonne D, Constantieux T, Rodriguez J. Org. Lett. 2010; 12: 5246
- 126 Hoashi Y, Okino T, Takemoto Y. Angew. Chem. Int. Ed. 2005; 44: 4032
- 127 Inokuma T, Hoashi Y, Takemoto Y. J. Am. Chem. Soc. 2006; 128: 9413
- 128 Zhang Y, Yu C, Ji Y, Wang W. Chem. Asian J. 2010; 5: 1303
- 129 Li X, Hu S, Xi Z, Zhang L, Luo S, Cheng JP. J. Org. Chem. 2010; 75: 8697
- 130 Pei Q.-L, Sun H.-W, Wu Z.-J, Du X.-L, Zhang X.-M, Yuan W.-C. J. Org. Chem. 2011; 76: 7849
- 131 Quintavalla A, Lanza F, Montroni E, Lombardo M, Trombini C. J. Org. Chem. 2013; 78: 12049
- 132 Sanchez-Duque MD. M, Baslé O, Isambert N, Gaudel-Siri A, Génisson Y, Plaquevent JC, Rodriguez J, Constantieux T. Org. Lett. 2011; 13: 3296
- 133 Li L, Guo J.-Y, Liu X.-G, Chen S, Wang Y, Tan B, Liu X.-Y. Org. Lett. 2014; 16: 6032
- 134 Azuma T, Murata A, Kobayashi Y, Inokuma T, Takemoto Y. Org. Lett. 2014; 16: 4256
- 135 Sohtome Y, Tanatani A, Hashimoto Y, Nagasawa K. Chem. Pharm. Bull. 2004; 52: 477
- 136 Shi M, Zhang W. Adv. Synth. Catal. 2005; 347: 535
- 137 Tsogoeva SB, Yalalov DA, Hateley MJ, Weckbecker C, Huthmacher K. Eur. J. Org. Chem. 2005; 2005: 4995
- 138 Gallo V, Giardina-papa D, Mastrorilli P, Francesco C, Paolo G, Wang Y. J. Organomet. Chem. 2005; 690: 3535
- 139 Evans DA, Seidel D. J. Am. Chem. Soc. 2005; 127: 9958
- 140 Evans DA, Mito S, Seidel D. J. Am. Chem. Soc. 2007; 129: 11583
- 141 Chen J.-B, Chen J.-C, Xie Y, Zhang H.-B. Angew. Chem. Int. Ed. 2012; 51: 1024
- 142 Kang SH, Kim DY. Bull. Korean Chem. Soc. 2009; 30: 1439
- 143 Kwon SJ, Suh CW, Kim SM, Kim DY. Bull. Korean Chem. Soc. 2015; 36: 1947
- 144 Lee HJ, Kim SM, Kim DY. Tetrahedron Lett. 2012; 53: 3437
- 145 Reznikov AN, Sibiryakova AE, Klimochkin YN. Russ. J. Gen. Chem. 2014; 84: 2280
- 146 Reznikov AN, Sibiryakova AE, Rybakov VB, Klimochkin YN. Tetrahedron: Asymmetry 2015; 26: 1050
- 147 Sung HJ, Mang JY, Kim DY. J. Fluorine Chem. 2015; 178: 40
- 148 Fallan C, Lam HW. Chem. Eur. J. 2012; 18: 11214
- 149 Chen WY, Ouyang L, Chen RY, Li XS. Tetrahedron Lett. 2010; 51: 3972
- 150 Li X, Li X, Peng F, Shao Z. Adv. Synth. Catal. 2012; 354: 2873
- 151 Li X, Peng F, Zhou M, Mo M, Zhao R, Shao Z. Chem. Commun. 2014; 50: 1745
- 152 Huang H, Jacobsen EN. J. Am. Chem. Soc. 2006; 128: 7170
- 153 Liu K, Cui HF, Nie J, Dong KY, Li XJ, Ma JA. Org. Lett. 2007; 9: 923
- 154 Li XJ, Liu K, Ma H, Nie J, Ma J.-A. Synlett 2008; 3242
- 155 Hai M, Liu K, Zhang FG, Zhu CL, Nie J, Ma J.-A. J. Org. Chem. 2010; 75: 1402
- 156 Xue F, Zhang S, Duan W, Wang W. Adv. Synth. Catal. 2008; 350: 2194
- 157 Santoro F, Althaus M, Bonaccorsi C, Gischig S, Mezzetti A. Organometallics 2008; 27: 3866
- 158 Gu Q, Guo X, Wu X. Tetrahedron 2009; 65: 5265
- 159 Liu S, Zhang X, Lao J, Yan M. ARKIVOC 2009; (vii): 268
- 160 Li B, Wang Y, Luo S, Zhong A, Li Z. Eur. J. Org. Chem. 2010; 2010: 656
- 161 Lalonde MP, Chen Y, Jacobsen EN. Angew. Chem. Int. Ed. 2006; 45: 6366
- 162 Zhang X, Liu S, Lao J, Du G, Yan M, Chan AS. C. Tetrahedron: Asymmetry 2009; 20: 1451
- 163 Lao J, Zhang X, Wang J, Li X, Yan M, Luo H. Tetrahedron: Asymmetry 2009; 20: 2818
- 164 Chen J, Zou Y, Fu L, Ren F, Tan F, Xiao W. Tetrahedron 2010; 66: 5367
- 165 Ma Z, Liu Y, Zhang W, Tao Y, Zhu Y. Eur. J. Org. Chem. 2011; 2011: 6747
- 166 Martínez-Guillén JR, Flores-Ferrándiz J, Gómez C, Gómez-Bengoa E, Chinchilla R. Molecules 2018; 23: 141
- 167 Uehara H, Barbas CF. III. Angew. Chem. Int. Ed. 2009; 48: 9848
- 168 Čmelová P, Vargová D, Šebesta R. J. Org. Chem. 2021; 86: 581
- 169 Zhang Z.-H, Dong X.-Q, Chen D, Wang C.-J. Chem. Eur. J. 2008; 14: 8780
- 170 Dong X.-Q, Teng H.-L, Wang C.-J. Org. Lett. 2009; 11: 1265
- 171 Sun Z.-W, Peng F.-Z, Li Z.-Q, Zou L.-W, Zhang S.-X, Li X, Shao Z.-H. J. Org. Chem. 2012; 77: 4103
- 172 Dong X.-Q, Fang X, Tao H.-Y, Zhou X, Wang C.-J. Adv. Synth. Catal. 2012; 354: 1141
- 173 Dong X.-Q, Fang X, Wang C.-J. Org. Lett. 2011; 13: 4426
- 174 Fang X, Li J, Wang C.-J. Org. Lett. 2013; 15: 3448
- 175 Yao L, Liu K, Tao H.-Y, Qiu G.-F, Zhou X, Wang C.-J. Chem. Commun. 2013; 49: 6078
- 176 Li P, Wang Y, Liang X, Ye J. Chem. Commun. 2008; 3302
- 177 Li P, Wen S, Yu F, Liu Q, Li W, Wang Y, Liang X, Ye J. Org. Lett. 2009; 11: 753
- 178 Zhang Z, Xie S, Cheng B, Zhai H, Li Y. J. Am. Chem. Soc. 2019; 141: 7147
- 179 Zhou Y, Li X, Li W, Wu C, Liang X, Ye J. Synlett 2010; 2357
- 180 Yang J, Li W, Jin Z, Liang X, Ye J. Org. Lett. 2010; 12: 5218
- 181 Cheng S, Zhao L, Yu S. Adv. Synth. Catal. 2014; 356: 982
- 182 Moritaka M, Miyamae N, Nakano K, Ichikawa Y, Kotsuki H. Synlett 2012; 23: 2554
- 183 Hirashima S, Sakai T, Nakashima K, Watanabe N, Koseki Y, Mukai K, Kanada Y, Tada N, Itoh A, Miura T. Tetrahedron Lett. 2014; 55: 4334
- 184 Pakulska AM, Kwiatkowski P. Org. Lett. 2012; 14: 4222
- 185 Kotsuki H. Org. Biomol. Chem. 2014; 12: 5847
- 186 Li X, Lu M, Dong Y, Wu W, Qian Q, Ye J, Dixon DJ. Nat. Commun. 2014; 5: 4479
- 187 Peng F.-Z, Shao Z.-H, Fan B.-M, Song H, Li G.-P, Zhang H.-B. J. Org. Chem. 2008; 73: 5202
- 188 Oh Y, Kim SM, Kim DY. Tetrahedron Lett. 2009; 50: 4674
- 189 Bui T, Syed S, Barbas CF. III. J. Am. Chem. Soc. 2009; 131: 8758
- 190 Kimmel KL, Robak MA. T, Ellman JA. J. Am. Chem. Soc. 2009; 131: 8754
- 191 Kimmel KL, Robak MT, Thomas S, Lee M, Ellman JA. Tetrahedron 2012; 68: 2704
- 192 Jiang X, Zhang Y, Chan AS. C, Wang R. Org. Lett. 2009; 11: 153
- 193 Almaşi D, Alonso DA, Gómez-Bengoa E, Nájera C. J. Org. Chem. 2009; 74: 6163
- 194 Mei K, Jin M, Zhang S, Li P, Liu W, Chen X, Xue F, Duan W, Wang W. Org. Lett. 2009; 11: 2864
- 195 Li X, Luo S, Cheng JP. Chem. Eur. J. 2010; 16: 14290
- 196 Wang J, Qi C, Ge Z, Cheng T, Li R. Chem. Commun. 2010; 46: 2124
- 197 Pattison G, Piraux G, Lam HW. J. Am. Chem. Soc. 2010; 132: 14373
- 198 Xue F, Liu L, Zhang S, Duan W, Wang W. Chem. Eur. J. 2010; 16: 7979
- 199 Bai J.-F, Peng L, Wang L.-l, Wang L.-X, Xu X.-Y. Tetrahedron 2010; 66: 8928
- 200 Yiǧit M. Molecules 2009; 14: 2032
- 201 Ma Z, Liu Y, Li P, Ren H, Zhu Y, Tao J. Tetrahedron: Asymmetry 2011; 22: 1740
- 202 Miura T, Nishida S, Masuda A, Tada N, Itoh A. Tetrahedron Lett. 2011; 52: 4158
- 203 Flores-Ferrándiz J, Fiser B, Gómez-Bengoa E, Chinchilla R. Eur. J. Org. Chem. 2015; 2015: 1218
- 204 Vízcaíno-Milla P, Sansano JM, Nájera C, Fiser B, Gómez-Bengoa E. Synthesis 2015; 47: 2199
- 205 Gómez-Torres E, Alonso DA, Gómez-Bengoa E, Nájera C. Org. Lett. 2011; 13: 6106
- 206 Lu R.-J, Yan Y.-Y, Wang J.-J, Du Q.-S, Nie S.-Z, Yan M. J. Org. Chem. 2011; 76: 6230
- 207 Bai J.-F, Wang L.-L, Peng L, Guo Y.-L, Jia L.-N, Tian F, He G.-Y, Xu X.-Y, Wang L.-X. J. Org. Chem. 2012; 77: 2947
- 208 Sim JH, Park JH, Maity P, Song CE. Org. Lett. 2019; 21: 6715
- 209 Wu H, Tian Z, Zhang L, Huang Y, Wang Y. Adv. Synth. Catal. 2012; 354: 2977
- 210 Singha Roy SJ, Mukherjee S. J. Org. Chem. 2018; 83: 12071
- 211 Kasaplar P, Riente P, Hartmann C, Pericàs MA. Adv. Synth. Catal. 2012; 354: 2905
- 212 Manna MS, Mukherjee S. Chem. Eur. J. 2012; 18: 15277
- 213 Manna MS, Mukherjee S. Chem. Sci. 2014; 5: 1627
- 214 Simlandy AK, Mukherjee S. Org. Biomol. Chem. 2016; 14: 5659
- 215 Isik M, Tanyeli C. J. Org. Chem. 2013; 78: 1604
- 216 Işk M, Unver MY, Tanyeli C. J. Org. Chem. 2015; 80: 828
- 217 Yang KS, Nibbs AE, Türkmen YE, Rawal VH. J. Am. Chem. Soc. 2013; 135: 16050
- 218 Popova EA, Pronina YA, Davtian AV, Nepochatyi GD, Petrov ML, Boitsov VM, Stepakov AV. Russ. J. Gen. Chem. 2022; 92: 287
- 219 Hart AP, Degraw CJ, Rustin GJ, Donahue MG, Pigza JA. J. Org. Chem. 2023; 88: 16666
- 220 Guo W, Wu B, Zhou X, Chen P, Wang X, Zhou YG, Liu Y, Li C. Angew. Chem. Int. Ed. 2015; 54: 4522
- 221 Lai X, Zha G, Liu W, Xu Y, Sun P, Xia T, Shen Y. Synlett 2016; 27: 1983
- 222 Kuchurov IV, Nigmatov AG, Kryuchkova EV, Kostenko AA, Kucherenko AS, Zlotin SG. Green Chem. 2014; 16: 1521
- 223 Ding R, Wolf C. Org. Lett. 2018; 20: 892
- 224 Yu JS, Liao FM, Gao WM, Liao K, Zuo RL, Zhou J. Angew. Chem. Int. Ed. 2015; 54: 7381
- 225 Yang D, Li D, Wang L, Zhao D, Wang R. J. Org. Chem. 2015; 80: 4336
- 226 Jiménez EI, Vallejo Narváez WE, Román-Chavarría CA, Vazquez-Chavez J, Rocha-Rinza T, Hernández-Rodríguez M. J. Org. Chem. 2016; 81: 7419
- 227 Hayama N, Azuma T, Kobayashi Y, Takemoto Y. Chem. Pharm. Bull. 2016; 64: 704
- 228 Hayama N, Kuramoto R, Földes T, Nishibayashi K, Kobayashi Y, Pápai I, Takemoto Y. J. Am. Chem. Soc. 2018; 140: 12216
- 229 Michigami K, Murakami H, Nakamura T, Hayama N, Takemoto Y. Org. Biomol. Chem. 2019; 17: 2331
- 230 Rombola M, Sumaria CS, Montgomery TD, Rawal VH. J. Am. Chem. Soc. 2017; 139: 5297
- 231 Rombola M, Rawal VH. Org. Lett. 2018; 20: 514
- 232 Tukhvatshin RS, Kucherenko AS, Nelyubina YV, Zlotin SG. ACS Catal. 2017; 7: 2981
- 233 Kucherenko AS, Kostenko AA, Komogortsev AN, Lichitsky BV, Fedotov MY, Zlotin SG. J. Org. Chem. 2019; 84: 4304
- 234 Modrocká V, Veverková E, Mečiarová M, Šebesta R. J. Org. Chem. 2018; 83: 13111
- 235 Lin Y, Hirschi WJ, Kunadia A, Paul A, Ghiviriga I, Abboud KA, Karugu RW, Vetticatt MJ, Hirschi JS, Seidel D. J. Am. Chem. Soc. 2020; 142: 5627
- 236 Zhu Y, Wang Q, Cornwall RG, Shi Y. Chem. Rev. 2014; 114: 8199
- 237 Jacobsen EN, Zhang W, Muci AR, Ecker JR, Deng L. J. Am. Chem. Soc. 1991; 113: 7063
- 238 Lee NH, Muci AR, Jacobsen EN. Tetrahedron Lett. 1991; 32: 5055
- 239 Lee NH, Jacobsen EN. Tetrahedron Lett. 1991; 32: 6533
- 240 Brandes BD, Jacobsen EN. J. Org. Chem. 1994; 59: 4378
- 241 Deng L, Jacobsen EN. J. Org. Chem. 1992; 57: 4320
- 242 Chang S, Lee NH, Jacobsen EN. J. Org. Chem. 1993; 58: 6939
- 243 Maligres PE, Upadhyay V, Rossen K, Cianciosi SJ, Purick RM, Eng KK, Reamer RA, Askin D, Volante RP, Reider PJ. Tetrahedron Lett. 1995; 36: 2195
- 244 Adam W, Fell RT, Mock-Knoblauch C, Saha-Möller CR. Tetrahedron Lett. 1996; 37: 6531
- 245 Kurti L, Blewett MM, Corey EJ. Org. Lett. 2009; 11: 4592
- 246 Yamada T, Imagawa K, Nagata T, Mukaiyama T. Chem. Lett. 1992; 21: 2231
- 247 Hosoya N, Hatayama A, Irie R, Sasaki H, Katsuki T. Tetrahedron 1994; 50: 4311
- 248 Kuroki T, Hamada T, Katsuki T. Chem. Lett. 1995; 24: 339
- 249 Hosoya N, Irie R, Katsuki T. Synlett 1993; 261
- 250 Hosoya N, Hatayama A, Yanai K, Fujii H, Irie R, Katsuki T. Synlett 1993; 641
- 251 Nishikori H, Ohta C, Katsuki T. Synlett 2000; 1557
- 252 Hentemann MF, Fuchs PL. Tetrahedron Lett. 1997; 38: 5615
- 253 Tokunaga M, Larrow JF, Kakiuchi F, Jacobsen EN. Science 1997; 277: 936
- 254 Ford DD, Nielsen LP. C, Zuend SJ, Musgrave CB, Jacobsen EN. J. Am. Chem. Soc. 2013; 135: 15595
- 255 Stoop RM, Mezzetti A. Green Chem. 1999; 1: 39
- 256 Stoop RM, Bachmann S, Valentini M, Mezzetti A. Organometallics 2000; 19: 4117
- 257 Kureshy RI, Khan NH, Abdi SH. R, Iyer P. J. Mol. Catal. A: Chem. 1997; 124: 91
- 258 Bousquet C, Gilheany DG. Tetrahedron Lett. 1995; 36: 7739
- 259 Daly AM, Renehan MF, Gilheany DG. Org. Lett. 2001; 3: 663
- 260 O’Mahony CP, McGarrigle EM, Renehan MF, Ryan KM, Kerrigan NJ, Bousquet C, Gilheany DG. Org. Lett. 2001; 3: 3435
- 261 McGarrigle EM, Murphy DM, Gilheany DG. Tetrahedron: Asymmetry 2004; 15: 1343
- 262 Murphy A, Dubois G, Stack TD. P. J. Am. Chem. Soc. 2003; 125: 5250
- 263 Murphy A, Pace A, Stack TD. P. Org. Lett. 2004; 6: 3119
- 264 Murphy A, Stack TD. P. J. Mol. Catal. A: Chem. 2006; 251: 78
- 265 Matsumoto K, Sawada Y, Saito B, Sakai K, Katsuki T, Matsumoto K. Angew. Chem. Int. Ed. 2005; 44: 4935
- 266 Shimada Y, Kondo S, Ohara Y, Matsumoto K, Katsuki T. Synlett 2007; 2445
- 267 Matsumoto K, Kubo T, Katsuki T. Chem. Eur. J. 2009; 15: 6573
- 268 Matsumoto K, Feng C, Handa S, Oguma T, Katsuki T. Tetrahedron 2011; 67: 6474
- 269 Sawada Y, Matsumoto K, Katsuki T. Angew. Chem. Int. Ed. 2007; 46: 4559
- 270 Sawada Y, Matsumoto K, Kondo S, Watanabe H, Ozawa T, Suzuki K, Saito B, Katsuki T. Angew. Chem. Int. Ed. 2006; 45: 3478
- 271 Matsumoto K, Sawada Y, Katsuki T. Synlett 2006; 3545
- 272 Koya S, Nishioka Y, Mizoguchi H, Uchida T, Katsuki T. Angew. Chem. Int. Ed. 2012; 51: 8243
- 273 Barlan AU, Basak A, Yamamoto H. Angew. Chem. Int. Ed. 2006; 45: 5849
- 274 Barlan AU, Zhang W, Yamamoto H. Tetrahedron 2007; 63: 6075
- 275 Gómez L, Garcia-Bosch I, Company A, Sala X, Fontrodona X, Ribas X, Costas M. Dalton Trans. 2007; 5539
- 276 Berkessel A, Brandenburg M, Leitterstorf E, Frey J, Lex J, Schäfer M. Adv. Synth. Catal. 2007; 349: 2385
- 277 Berkessel A, Günther T, Wang Q, Neudörfl J.-M. Angew. Chem. Int. Ed. 2013; 52: 8467
- 278 Wang Q, Neudörfl J.-M, Berkessel A. Chem. Eur. J. 2015; 21: 247
- 279 Lansing M, Engler H, Leuther TM, Neudörfl J.-M, Berkessel A. ChemCatChem 2016; 8: 3706
- 280 Berkessel A, Ong MC, Nachi M, Neudörfl J.-M. ChemCatChem 2010; 2: 1215
- 281 Bose DS, Reddy AV. N, Srikanth B. Synthesis 2008; 2323
- 282 Chen Y, Evarts JB, Torres E, Fuchs PL. Org. Lett. 2002; 4: 3571
- 283 El-Awa A, Fuchs P. Org. Lett. 2006; 8: 2905
- 284 El-Awa A, Du Jourdin XM, Fuchs PL. J. Am. Chem. Soc. 2007; 129: 9086
- 285 Hong WP, Noshi MN, El-Awa A, Fuchs PL. Org. Lett. 2011; 13: 6342
- 286 Ebrahimian GR, Du Jourdin XM, Fuchs PL. Org. Lett. 2012; 14: 2630
- 287 Sikervar V, Fleet JC, Fuchs PL. Chem. Commun. 2012; 48: 9077
- 288 Wu M, Wang B, Wang S, Xia C, Sun W. Org. Lett. 2009; 11: 3622
- 289 Miao C, Wang B, Wang Y, Xia C, Lee YM, Nam W, Sun W. J. Am. Chem. Soc. 2016; 138: 936
- 290 Wang B, Miao C, Wang S, Xia C, Sun W. Chem. Eur. J. 2012; 18: 6750
- 291 Shen D, Miao C, Wang S, Xia C, Sun W. Eur. J. Inorg. Chem. 2014; 2014: 5777
- 292 Shen D, Qiu B, Xu D, Miao C, Xia C, Sun W. Org. Lett. 2016; 18: 372
- 293 Miao C, Yan X, Xu D, Xia C, Sun W. Adv. Synth. Catal. 2017; 359: 476
- 294 Wu M, Miao CX, Wang S, Hu X, Xia C, Kühn FE, Sun W. Adv. Synth. Catal. 2011; 353: 3014
- 295 Wang B, Wang S, Xia C, Sun W. Chem. Eur. J. 2012; 18: 7332
- 296 Xiong D, Hu X, Wang S, Miao CX, Xia C, Sun W. Eur. J. Org. Chem. 2011; 2011: 4289
- 297 Xiong D, Wu M, Wang S, Li F, Xia C, Sun W. Tetrahedron: Asymmetry 2010; 21: 374
- 298 Jat JL, De S R, Kumar G, Adebesin AM, Gandham SK, Falck JR. Org. Lett. 2015; 17: 1058
- 299 Ottenbacher RV, Bryliakov KP, Talsi EP. Adv. Synth. Catal. 2011; 353: 885
- 300 Garcia-Bosch I, Gómez L, Polo A, Ribas X, Costas M. Adv. Synth. Catal. 2012; 354: 65
- 301 Cussó O, Garcia-Bosch I, Font D, Ribas X, Lloret-Fillol J, Costas M. Org. Lett. 2013; 15: 6158
- 302 Lin J, Miao C, Wang F, Yang P, Sun Q, Sun W. ACS Catal. 2020; 10: 11857
- 303 Castro AM. M. Chem. Rev. 2004; 104: 2939
- 304 The Claisen Rearrangement: Methods and Applications . Hiersemann M, Nubbemeyer U. Wiley-VCH; Weinheim: 2007
- 305 Denmark SE, Stadler H, Dorow RL, Kim JH. J. Org. Chem. 1991; 56: 5063
- 306 Uyeda C, Jacobsen EN. J. Am. Chem. Soc. 2008; 130: 9228
- 307 Uyeda C, Rötheli AR, Jacobsen EN. Angew. Chem. Int. Ed. 2010; 49: 9753
- 308 Uyeda C, Jacobsen EN. J. Am. Chem. Soc. 2011; 133: 5062
- 309 Cetin A. Lett. Org. Chem. 2019; 17: 571
- 310 Takahashi H, Kawakita T, Ohno M, Yoshioka M, Kobayashi S. Tetrahedron 1992; 48: 5691
- 311 Takahashi H, Kawakita T, Yoshioka M, Kobayashi S, Ohno M. Tetrahedron Lett. 1989; 30: 7095
- 312 Yoshioka M, Kawakita T, Ohno M. Tetrahedron Lett. 1989; 30: 1657
- 313 Knochel P, Singer RD. Chem. Rev. 1993; 93: 2117
- 314 Rozema MJ, Sidduri AR, Knochel P. J. Org. Chem. 1992; 57: 1956
- 315 Rozema MJ, Eisenberg C, Lütjens H, Ostwald R, Belyk K, Knochel P. Tetrahedron Lett. 1993; 34: 3115
- 316 Nowotny S, Vettel S, Knochel P. Tetrahedron Lett. 1994; 35: 4539
- 317 Eisenberg C, Knochel P. J. Org. Chem. 1994; 59: 3760
- 318 Lütjens H, Knochel P. Tetrahedron: Asymmetry 1994; 5: 1161
- 319 Knochel P, Brieden W, Rozema MJ, Eisenberg C. Tetrahedron Lett. 1993; 34: 5881
- 320 Ostwald R, Chavant PY, Stadtmüller H, Knochel P. J. Org. Chem. 1994; 59: 4143
- 321 Zhang X, Guo C. Tetrahedron Lett. 1995; 36: 4947
- 322 Shono T, Kise N, Shirakawa E, Matsumoto H, Okazaki E. J. Org. Chem. 1991; 56: 3063
- 323 Pritchett S, Woodmansee DH, Gantzel P, Walsh PJ. J. Am. Chem. Soc. 1998; 120: 6423
- 324 Balsells J, Walsh PJ. J. Am. Chem. Soc. 2000; 122: 1802
- 325 DiMauro EF, Kozlowski MC. Org. Lett. 2001; 3: 3053
- 326 Costa AM, Jimeno C, Gavenonis J, Carroll PJ, Walsh PJ. J. Am. Chem. Soc. 2002; 124: 6929
- 327 García C, LaRochelle LK, Walsh PJ. J. Am. Chem. Soc. 2002; 124: 10970
- 328 García C, Walsh PJ. Org. Lett. 2003; 5: 3641
- 329 Li H, Walsh PJ. J. Am. Chem. Soc. 2004; 126: 6538
- 330 Jeon SJ, Li H, Walsh PJ. J. Am. Chem. Soc. 2005; 127: 16416
- 331 Forrat VJ, Prieto O, Ramón DJ, Yus M. Chem. Eur. J. 2006; 12: 4431
- 332 DiMauro EF, Kozlowski MC. J. Am. Chem. Soc. 2002; 124: 12668
- 333 Shimizu K, Uetsu H, Gotanda T, Ito K. Synlett 2015; 26: 1238
- 334 Kavanagh SE, Gilheany DG. Org. Lett. 2020; 22: 8198
- 335 Bieszczad B, Gilheany DG. Angew. Chem. Int. Ed. 2017; 56: 4272
- 336 Cozzi PG. Angew. Chem. Int. Ed. 2003; 42: 2895
- 337 Cozzi PG, Kotrusz P. J. Am. Chem. Soc. 2006; 128: 4940
- 338 Cozzi PG. Angew. Chem. Int. Ed. 2006; 45: 2951
- 339 Pathak K, Bhatt AP, Abdi SH. R, Kureshy RI, Khan NU. H, Ahmad I, Jasra RV. Chirality 2007; 19: 82
- 340 Shen C, Chen L, Tang J, Xu M. Chin. J. Chem. 2009; 27: 413
- 341 Li Z.-B, Liu T.-D, Pu L. J. Org. Chem. 2007; 72: 4340
- 342 Li F.-Q, Zhong S, Lu G, Chan AS. C. Adv. Synth. Catal. 2009; 351: 1955
- 343 North M, Usanov DL, Young C. Chem. Rev. 2008; 108: 5146
- 344 North M, Orizu C, Tararov VI, Ikonnikov NS, Belokon YN, Hibbs DE, Hursthouse MB, Malik KM. A. Chem. Commun. 1998; 387
- 345 Belokon YN, Caveda-Cepas S, Green B, Ikonnikov NS, Khrustalev VN, Larichev VS, Moscalenko MA, North M, Orizu C, Tararov VI, Tasinazzo M, Timofeeva GI, Yashkina LV. J. Am. Chem. Soc. 1999; 121: 3968
- 346 Belokon’ YN, Green B, Ikonnikov NS, Larichev VS, Lokshin BV, Moscalenko MA, North M, Orizu C, Peregudov AS, Timofeeva GI. Eur. J. Org. Chem. 2000; 2000: 2655
- 347 Belokon YN, North M, Parsons T. Org. Lett. 2000; 2: 1617
- 348 Belokon YN, Green B, Ikonnikov NS, North M, Parsons T, Tararov VI. Tetrahedron 2001; 57: 771
- 349 Belokon YN, Carta P, Gutnov AV, Maleev V, Moskalenko MA, Yashkina LV, Ikonnikov NS, Voskoboev NV, Khrustalev VN, North M. Helv. Chim. Acta 2002; 85: 3301
- 350 Kim SS, Song DH. Eur. J. Org. Chem. 2005; 2005: 1777
- 351 Belokon YN, Maleev VI, North M, Usanov DL. Chem. Commun. 2006; 4614
- 352 Chen SK, Peng D, Zhou H, Wang LW, Chen FX, Feng XM. Eur. J. Org. Chem. 2007; 2007: 639
- 353 Khan N.-UH, Agrawal S, Kureshy RI, Abdi SH. R, Jeya Prathap K, Jasra RV. Eur. J. Org. Chem. 2008; 2008: 4511
- 354 Khan N.-UH, Agrawal S, Kureshy RI, Abdi SH. R, Pathak K, Bajaj HC. Chirality 2010; 22: 153
- 355 Wen YQ, Ren WM, Lu XB. Org. Biomol. Chem. 2011; 9: 6323
- 356 Qu Y, Jing L, Wu Z, Wu D, Zhou X. Tetrahedron: Asymmetry 2010; 21: 187
- 357 Zhang Z, Lippert KM, Hausmann H, Kotke M, Schreiner PR. J. Org. Chem. 2011; 76: 9764
- 358 Wei Y.-L, Huang W.-S, Cui Y.-M, Yang K.-F, Xu Z, Xu L.-W. RSC Adv. 2015; 5: 3098
- 359 Alaaeddine A, Roisnel T, Thomas CM, Carpentiera JF. Adv. Synth. Catal. 2008; 350: 731
- 360 Zeng X.-P, Cao Z.-Y, Wang X, Chen L, Zhou F, Zhu F, Wang C.-H, Zhou J. J. Am. Chem. Soc. 2016; 138: 416
- 361 Suen LM, Steigerwald ML, Leighton JL. Chem. Sci. 2013; 4: 2413
- 362 Trost BM, Van Vranken DL. Chem. Rev. 1996; 96: 395
- 363 Tsuji J, Takahashi H, Morikawa M. Tetrahedron Lett. 1965; 6: 4387
- 364 James J, Jackson M, Guiry PJ. Adv. Synth. Catal. 2019; 361: 3016
- 365 Trost BM, Fullerton TJ. J. Am. Chem. Soc. 1973; 95: 292
- 366 Butts CP, Filali E, Lloyd-Jones GC, Norrby PO, Sale DA, Schramm Y. J. Am. Chem. Soc. 2009; 131: 9945
- 367 Trost BM. Org. Process Res. Dev. 2012; 16: 185
- 368 Trost BM. J. Org. Chem. 2004; 69: 5813
- 369 Trost BM, Machacek MR, Aponick A. Acc. Chem. Res. 2006; 39: 747
- 370 Trost BM, Schultz JE. Synthesis 2019; 51: 1
- 371 Weaver JD, Recio A, Grenning AJ, Tunge JA. Chem. Rev. 2011; 111: 1846
- 372 Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA. J. Am. Chem. Soc. 2012; 134: 19050
- 373 Trost BM, Van Vranken DL, Bingel C. J. Am. Chem. Soc. 1992; 114: 9327
- 374 Trost BM, Zambrano JL, Richter W. Synlett 2001; 907
- 375 Trost BM. Chem. Pharm. Bull. 2002; 50: 1
- 376 Trost BM, Van Vranken DL. J. Am. Chem. Soc. 1993; 115: 444
- 377 Trost BM, Van Vranken DL. Angew. Chem., Int. Ed. Engl. 1992; 31: 228
- 378 Trost BM, Li L, Guile SD, Pulley SR, Shi Z, Madsen R. J. Org. Chem. 1998; 63: 1339
- 379 Trost BM, Pulley SR. J. Am. Chem. Soc. 1995; 117: 10143
- 380 Trost BM, Cook GR. Tetrahedron Lett. 1996; 37: 7485
- 381 Trost BM, Pulley SR. Tetrahedron Lett. 1995; 36: 8737
- 382 Trost BM. Chem. Eur. J. 2001; 7: 1619
- 383 Stragies R, Blechert S. J. Am. Chem. Soc. 2000; 122: 9584
- 384 Trost BM, Toste FD. J. Am. Chem. Soc. 1999; 121: 3543
- 385 Trost BM, Lee C. J. Am. Chem. Soc. 2001; 123: 12191
- 386 Zhou H, Yang H, Liu M, Xia C, Jiang G. Org. Lett. 2014; 16: 5350
- 387 Glorius F, Pfaltz A. Org. Lett. 1999; 1: 141
- 388 Trost BM, Sacchi KL, Schroeder GM, Asakawa N. Org. Lett. 2002; 4: 3427
- 389 Trost BM, Dogra K. J. Am. Chem. Soc. 2002; 124: 7256
- 390 Trost BM, Krische MJ, Berl V, Grenzer EM. Org. Lett. 2002; 4: 2005
- 391 Krska SW, Hughes DL, Reamer RA, Mathre DJ, Sun Y, Trost BM. J. Am. Chem. Soc. 2002; 124: 12656
- 392 Trost BM, Shen HC, Dong L, Surivet JP. J. Am. Chem. Soc. 2003; 125: 9276
- 393 Trost BM, Shen HC, Dong L, Surivet JP, Sylvain C. J. Am. Chem. Soc. 2004; 126: 11966
- 394 Bonnet LG, Douthwaite RE, Kariuki BM. Organometallics 2003; 22: 4187
- 395 Trost BM, Jiang C. Org. Lett. 2003; 5: 1563
- 396 Trost BM, Jäkel C, Plietker B. J. Am. Chem. Soc. 2003; 125: 4438
- 397 Trost BM, Fandrick DR, Dinh DC. J. Am. Chem. Soc. 2005; 127: 14186
- 398 Lüssem BJ, Gais HJ. J. Am. Chem. Soc. 2003; 125: 6066
- 399 Belda O, Lundgren S, Moberg C. Org. Lett. 2003; 5: 2275
- 400 Trost BM, Pissot-Soldermann C, Chen I, Schroeder GM. J. Am. Chem. Soc. 2004; 126: 4480
- 401 Lüssem BJ, Gais HJ. J. Org. Chem. 2004; 69: 4041
- 402 Jagusch T, Gais HJ, Bondarev O. J. Org. Chem. 2004; 69: 2731
- 403 Alibés R, Bayón P, de March P, Figueredo M, Font J, García-García E, González-Gálvez D. Org. Lett. 2005; 7: 5107
- 404 González-Gálvez D, García-García E, Alibés R, Bayón P, de March P, Figueredo M, Font J. J. Org. Chem. 2009; 74: 6199
- 405 Yan XX, Liang CG, Zhang Y, Hong W, Cao BX, Dai LX, Hou XL. Angew. Chem. Int. Ed. 2005; 44: 6544
- 406 Trost BM, Zhang Y. J. Am. Chem. Soc. 2006; 128: 4590
- 407 Trost BM, Brennan MK. Org. Lett. 2006; 8: 2027
- 408 Trost BM, Aponick A. J. Am. Chem. Soc. 2006; 128: 3931
- 409 Zanoni G, Porta A, Brunoldi E, Vidari G. J. Org. Chem. 2006; 71: 8459
- 410 Trost BM, Dong G. Org. Lett. 2007; 9: 2357
- 411 Trost BM, Osipov M, Dong G. J. Am. Chem. Soc. 2010; 132: 15800
- 412 Trost BM, Brennan MK. Org. Lett. 2007; 9: 3961
- 413 Trost BM, Dogra K. Org. Lett. 2007; 9: 861
- 414 Trost BM, Zhang Y. J. Am. Chem. Soc. 2007; 129: 14548
- 415 Pelly SC, Govender S, Fernandes MA, Schmalz HG, de Koning CB. J. Org. Chem. 2007; 72: 2857
- 416 Trost BM, Xu J, Schmidt T. J. Am. Chem. Soc. 2008; 130: 11852
- 417 Hou XL, Zheng BH. Org. Lett. 2009; 11: 1789
- 418 Trost BM, Xie J, Sieber JD. J. Am. Chem. Soc. 2011; 133: 20611
- 419 Trost BM, Malhotra S, Chan WH. J. Am. Chem. Soc. 2011; 133: 7328
- 420 Jiang L, Jia T, Wang M, Liao J, Cao P. Org. Lett. 2015; 17: 1070
- 421 Hu J, Pan S, Zhu S, Yu P, Xu R, Zhong G, Zeng X. J. Org. Chem. 2020; 85: 7896
- 422 Olson DE, Maruniak A, Malhotra S, Trost BM, Du Bois J. Org. Lett. 2011; 13: 3336
- 423 Trost BM, Miller JR, Hoffman CM. J. Am. Chem. Soc. 2011; 133: 8165
- 424 Trost BM, Osipov M, Kaib PS. J, Sorum MT. Org. Lett. 2011; 13: 3222
- 425 Kukkadapu KK, Ouach A, Lozano P, Vaultier M, Pucheault M. Org. Lett. 2011; 13: 4132
- 426 Trost BM, Osipov M, Dong G. Org. Lett. 2012; 14: 2254
- 427 Trost BM, Dong G. Chem. Eur. J. 2009; 15: 6910
- 428 Trost BM, Kaneko T, Andersen NG, Tappertzhofen C, Fahr B. J. Am. Chem. Soc. 2012; 134: 18944
- 429 Mao B, Ji Y, Fañanás-Mastral M, Caroli G, Meetsma A, Feringa BL. Angew. Chem. Int. Ed. 2012; 51: 3168
- 430 Ulbrich K, Kreitmeier P, Vilaivan T, Reiser O. J. Org. Chem. 2013; 78: 4202
- 431 Uberman PM, Caira MR, Martín SE. Organometallics 2013; 32: 3220
- 432 Valli M, Bruno P, Sbarbada D, Porta A, Vidari G, Zanoni G. J. Org. Chem. 2013; 78: 5556
- 433 Vita MV, Caramenti P, Waser J. Org. Lett. 2015; 17: 5832
- 434 de Oliveira MN, Fournier J, Arseniyadis S, Cossy J. Org. Lett. 2017; 19: 14
- 435 Jang SH, Kim HW, Jeong W, Moon D, Rhee YH. Org. Lett. 2018; 20: 1248
- 436 Rajkumar S, Clarkson GJ, Shipman M. Org. Lett. 2017; 19: 2058
- 437 Clementson S, Jessing M, Pedersen H, Vital P, Kristensen JL. J. Am. Chem. Soc. 2019; 141: 8783
- 438 Song T, Arseniyadis S, Cossy J. Org. Lett. 2019; 21: 603
- 439 Aubert S, Katsina T, Arseniyadis S. Org. Lett. 2019; 21: 2231
- 440 Trost BM, Bai Y, Bai W.-J, Schultz JE. J. Am. Chem. Soc. 2019; 141: 4811
- 441 Trost BM, Schultz JE, Chang T, Maduabum MR. J. Am. Chem. Soc. 2019; 141: 9521
- 442 Pálvölgyi ÁM, Schnürch M, Bica-Schröder K. Tetrahedron 2020; 76: 131246
- 443 Khan S, Zhang J, Khan A. Org. Lett. 2024; 26: 2758
- 444 Lebel H, Marcoux JF, Molinaro C, Charette AB. Chem. Rev. 2003; 103: 977
- 445 Simmons HE, Smith RD. J. Am. Chem. Soc. 1958; 80: 5323
- 446 Simmons HE, Smith RD. J. Am. Chem. Soc. 1959; 81: 4256
- 447 Nozaki H, Moriuti S, Takaya H, Noyori R. Tetrahedron Lett. 1966; 7: 5239
- 448 Lowenthal RE, Abiko A, Masamune S. Tetrahedron Lett. 1990; 31: 6005
- 449 Evans DA, Woerpel KA, Hinman MM, Faul MM. J. Am. Chem. Soc. 1991; 113: 726
- 450 Takahashi H, Yoshioka M, Ohno M, Kobayashi S. Tetrahedron Lett. 1992; 33: 2575
- 451 Imai N, Sakamoto K, Takahashi H, Kobayashi S. Tetrahedron Lett. 1994; 35: 7045
- 452 Imai N, Takahashi H, Kobayashi S. Chem. Lett. 1994; 23: 177
- 453 Takahashi H, Yoshioka M, Shibasaki M, Ohno M, Imai N, Kobayashi S. Tetrahedron 1995; 51: 12013
- 454 Denmark SE, Christenson BL, Coe DM, O’Connor SP. Tetrahedron Lett. 1995; 36: 2215
- 455 Denmark SE, Christenson BL, O’Connor SP. Tetrahedron Lett. 1995; 36: 2219
- 456 Hanessian S, Andreotti D, Gomtsyan A. J. Am. Chem. Soc. 1995; 117: 10393
- 457 Hanessian S, Cantin LD, Roy S, Andreotti D, Gomtsyan A. Tetrahedron Lett. 1997; 38: 1103
- 458 Shepperson I, Quici S, Pozzi G, Nicoletti M, O’Hagan D. Eur. J. Org. Chem. 2004; 2004: 4545
- 459 Bayardon J, Sinou D, Holczknecht O, Mercs L, Pozzi G. Tetrahedron: Asymmetry 2005; 16: 2319
- 460 Bonaccorsi C, Mezzetti A. Organometallics 2005; 24: 4953
- 461 Bonaccorsi C, Santoro F, Gischig S, Mezzetti A. Organometallics 2006; 25: 2002
- 462 Kanchiku S, Suematsu H, Matsumoto K, Uchida T, Katsuki T. Angew. Chem. Int. Ed. 2007; 46: 3889
- 463 Suematsu H, Kanchiku S, Uchida T, Katsuki T. J. Am. Chem. Soc. 2008; 130: 10327
- 464 Ichinose M, Suematsu H, Katsuki T. Angew. Chem. Int. Ed. 2009; 48: 3121
- 465 Uehara M, Suematsu H, Yasutomi Y, Katsuki T. J. Am. Chem. Soc. 2011; 133: 170
- 466 Xu ZJ, Fang R, Zhao C, Huang JS, Li GY, Zhu N, Che CM. J. Am. Chem. Soc. 2009; 131: 4405
- 467 Morandi B, Mariampillai B, Carreira EM. Angew. Chem. Int. Ed. 2011; 50: 1101
- 468 Joshi-Pangu A, Cohen RD, Tudge MT, Chen Y. J. Org. Chem. 2016; 81: 3070
- 469 De N, Yoo EJ. ACS Catal. 2018; 8: 48
- 470 Masson G, Lalli C, Benohoud M, Dagousset G. Chem. Soc. Rev. 2013; 42: 902
- 471 Franz AK, Hanhan NV, Ball-Jones NR. ACS Catal. 2013; 3: 540
- 472 Jiang X, Wang R. Chem. Rev. 2013; 113: 5515
- 473 Evans DA, Lectka T, Miller SJ. Tetrahedron Lett. 1993; 34: 7027
- 474 Salahi F, Taghizadeh MJ, Arvinnezhad H, Moemeni M, Jadidi K, Notash B. Tetrahedron Lett. 2014; 55: 1515
- 475 Schaus SE, Brånalt J, Jacobsen EN. J. Org. Chem. 1998; 63: 403
- 476 Joly GD, Jacobsen EN. Org. Lett. 2002; 4: 1795
- 477 Du H, Zhang X, Wang Z, Ding K. Tetrahedron 2005; 61: 9465
- 478 Chaładaj W, Kwiatkowski P, Jurczak J. Tetrahedron Lett. 2008; 49: 6810
- 479 Zulauf A, Mellah M, Guillot R, Schulz E. Eur. J. Org. Chem. 2008; 2008: 2118
- 480 Aikawa K, Irie R, Katsuki T. Tetrahedron 2001; 57: 845
- 481 Eno S, Egami H, Uchida T, Katsuki T. Chem. Lett. 2008; 37: 632
- 482 Longmire JM, Wang B, Zhang X. J. Am. Chem. Soc. 2002; 124: 13400
- 483 Huang Y, Iwama T, Rawal VH. J. Am. Chem. Soc. 2000; 122: 7843
- 484 Huang Y, Iwama T, Rawal VH. Org. Lett. 2002; 4: 1163
- 485 Huang Y, Iwama T, Rawal VH. J. Am. Chem. Soc. 2002; 124: 5950
- 486 McGilvra JD, Rawal VH. Synlett 2004; 2440
- 487 Nicolaou KC, Tria GS, Edmonds DJ, Kar M. J. Am. Chem. Soc. 2009; 131: 15909
- 488 Sparrow K, Barker D, Brimble MA. Tetrahedron 2011; 67: 7989
- 489 Ohfusa T, Nishida A. Tetrahedron 2011; 67: 1893
- 490 Trost BM, Fandrick DR. J. Am. Chem. Soc. 2003; 125: 11836
- 491 Kubota K, Hamblett CL, Wang X, Leighton JL. Tetrahedron 2006; 62: 11397
- 492 Sanz MA, Voigt T, Waldmann H. Adv. Synth. Catal. 2006; 348: 1511
- 493 Du W, Liu Y.-K, Yue L, Chen Y.-C. Synlett 2008; 2997
- 494 Xie J, Yoshida K, Takasu K, Takemoto Y. Tetrahedron Lett. 2008; 49: 6910
- 495 Zeng X.-M, Meng C.-Y, Bao J.-X, Xu D.-C, Xie J.-W, Zhu W.-D. J. Org. Chem. 2015; 80: 11521
- 496 Esteban F, Cieślik W, Arpa EM, Guerrero-Corella A, Díaz-Tendero S, Perles J, Fernández-Salas JA, Fraile A, Alemán J. ACS Catal. 2018; 8: 1884
- 497 Zea A, Valero G, Alba A.-NR, Moyano A, Rios R. Adv. Synth. Catal. 2010; 352: 1102
- 498 Xie J.-W, Fan L.-P, Su H, Li X.-S, Xu D.-C. Org. Biomol. Chem. 2010; 8: 2117
- 499 Goudedranche S, Bugaut X, Constantieux T, Bonne D, Rodriguez J. Chem. Eur. J. 2014; 20: 410
- 500 Schotes C, Mezzetti A. J. Am. Chem. Soc. 2010; 132: 3652
- 501 Wei Q, Gong L.-Z. Org. Lett. 2010; 12: 1008
- 502 Sun W, Zhu G, Wu C, Li G, Hong L, Wang R. Angew. Chem. Int. Ed. 2013; 52: 8633
- 503 Trost BM, Morris PJ. Angew. Chem. Int. Ed. 2011; 50: 6167
- 504 Trost BM, Morris PJ, Sprague SJ. J. Am. Chem. Soc. 2012; 134: 17823
- 505 Li J, Li X, Zhou P, Zhang L, Luo S, Cheng J.-P. Eur. J. Org. Chem. 2009; 2009: 4486
- 506 Schotes C, Mezzetti A. Angew. Chem. Int. Ed. 2011; 50: 3072
- 507 Burns NZ, Witten MR, Jacobsen EN. J. Am. Chem. Soc. 2011; 133: 14578
- 508 Witten MR, Jacobsen EN. Angew. Chem. Int. Ed. 2014; 53: 5912
- 509 Wang L, Shi X.-M, Dong W.-P, Zhu L.-P, Wang R. Chem. Commun. 2013; 49: 3458
- 510 Tan B, Hernández-Torres G, Barbas CF. III. J. Am. Chem. Soc. 2011; 133: 12354
- 511 Yan C.-X, Yang F, Yang X, Zhou D.-G, Zhou P.-P. J. Org. Chem. 2017; 82: 3046
- 512 Shi Y, Lin A, Mao H, Mao Z, Li W, Hu H, Zhu C, Cheng Y. Chem. Eur. J. 2013; 19: 1914
- 513 Mayr F, Brimioulle R, Bach T. J. Org. Chem. 2016; 81: 6965
- 514 Jiang X, Shi X, Wang S, Sun T, Cao Y, Wang R. Angew. Chem. Int. Ed. 2012; 51: 2084
- 515 Jiang X, Wang L, Kai M, Zhu L, Yao X, Wang R. Chem. Eur. J. 2012; 18: 11465
- 516 Jiang X, Liu L, Zhang P, Zhong Y, Wang R. Angew. Chem. Int. Ed. 2013; 52: 11329
- 517 Wei F, Ren CL, Wang D, Liu L. Chem. Eur. J. 2015; 21: 2335
- 518 Lalonde MP, McGowan MA, Rajapaksa NS, Jacobsen EN. J. Am. Chem. Soc. 2013; 135: 1891
- 519 Huang N, Zou L, Peng Y. Org. Lett. 2017; 19: 5806
- 520 Qin J, Zhang Y, Liu C, Zhou J, Zhan R, Chen W, Huang H. Org. Lett. 2019; 21: 7337
- 521 Trost BM, Shinde AH, Wang Y, Zuo Z, Min C. ACS Catal. 2020; 10: 1969
- 522 Zhang X, Zhang C, Jiang B, Gao Y, Xu X, Miao Z. Org. Lett. 2022; 24: 3097
- 523 Zhang S, Luo Z, Wang W, Qian L, Liao J. Org. Lett. 2022; 24: 4645
- 524 Pellissier H. Adv. Synth. Catal. 2014; 356: 1899
- 525 Lowenthal RE, Masamune S. Tetrahedron Lett. 1991; 32: 7373
- 526 Evans DA, Faul MM, Bilodeau MT. J. Org. Chem. 1991; 56: 6744
- 527 Evans DA, Bilodeau MT, Faul MM. J. Am. Chem. Soc. 1994; 116: 2742
- 528 Li Z, Conser KR, Jacobsen EN. J. Am. Chem. Soc. 1993; 115: 5326
- 529 Li Z, Quan RW, Jacobsen EN. J. Am. Chem. Soc. 1995; 117: 5889
- 530 Estéoule A, Durán F, Retailleau P, Dodd RH, Dauban P. Synthesis 2007; 1251
- 531 Noda K, Hosoya N, Irie R, Ito Y, Katsuki T. Synlett 1993; 469
- 532 Nishikori H, Katsuki T. Tetrahedron Lett. 1996; 37: 9245
- 533 Omura K, Murakami M, Uchida T, Irie R, Katsuki T. Chem. Lett. 2003; 32: 354
- 534 Omura K, Uchida T, Irie R, Katsuki T. Chem. Commun. 2004; 2060
- 535 Kawabata H, Omura K, Katsuki T. Tetrahedron Lett. 2006; 47: 1571
- 536 Kawabata H, Omura K, Uchida T, Katsuki T. Chem. Asian J. 2007; 2: 248
- 537 Fukunaga Y, Uchida T, Ito Y, Matsumoto K, Katsuki T. Org. Lett. 2012; 14: 4658
- 538 O’Connor KJ, Wey SJ, Burrows CJ. Tetrahedron Lett. 1992; 33: 1001
- 539 Minakata S, Ando T, Nishimura M, Ryu I, Komatsu M. Angew. Chem. Int. Ed. 1998; 37: 3392
- 540 Nishimura M, Minakata S, Takahashi T, Oderaotoshi Y, Komatsu M. J. Org. Chem. 2002; 67: 2101
- 541 Nishimura M, Minakata S, Thongchant S, Ryu I, Komatsu M. Tetrahedron Lett. 2000; 41: 7089
- 542 Ho CM, Lau TC, Kwong HL, Wong WT. J. Chem. Soc., Dalton Trans. 1999; 4: 2411
- 543 De Fusco C, Fuoco T, Croce G, Lattanzi A. Org. Lett. 2012; 14: 4078
- 544 Ranocchiari M, Mezzetti A. Organometallics 2009; 28: 3611
- 545 Egloff J, Ranocchiari M, Schira A, Schotes C, Mezzetti A. Organometallics 2013; 32: 4690
- 546 Kim SK, Jacobsen EN. Angew. Chem. Int. Ed. 2004; 43: 3952
- 547 Kattuboina A, Li G. Tetrahedron Lett. 2008; 49: 1573
- 548 Noyori R, Ohkuma T. Angew. Chem. Int. Ed. 2001; 40: 40
- 549 Ohkuma T. Proc. Jpn. Acad., Ser. B 2010; 86: 202
- 550 Gamez P, Fache F, Lemaire M. Tetrahedron: Asymmetry 1995; 6: 705
- 551 Burns B, King NP, Studley JR, Tye H, Wills M. Tetrahedron: Asymmetry 1994; 5: 801
- 552 Püntener K, Schwink L, Knochel P. Tetrahedron Lett. 1996; 37: 8165
- 553 Gao JX, Ikariya T, Noyori R. Organometallics 1996; 15: 1087
- 554 Burk MJ, Hems W, Herzberg D, Malan C, Zanotti-Gerosa A. Org. Lett. 2000; 2: 4173
- 555 Mimoun H, de Saint Laumer JY, Giannini L, Scopelliti R, Floriani C. J. Am. Chem. Soc. 1999; 121: 6158
- 556 Abdur-Rashid K, Lough AJ, Morris RH. Organometallics 2001; 20: 1047
- 557 Lère-Porte JP, Moreau JJ. E, Serein-Spirau F, Wakim S. Tetrahedron Lett. 2001; 42: 3073
- 558 Brethon A, Moreau JJ. E, Man MW. C. Tetrahedron: Asymmetry 2004; 15: 495
- 559 Jiang D, Yang Q, Yang J, Zhang L, Zhu G, Su W, Li C. Chem. Mater. 2005; 17: 6154
- 560 Dong Z.-R, Li Y.-Y, Chen J.-S, Li B.-Z, Xing Y, Gao J.-X. Org. Lett. 2005; 7: 1043
- 561 Li Y.-Y, Zhang H, Chen J.-S, Liao X.-L, Dong Z.-R, Gao J.-X. J. Mol. Catal. A: Chem. 2004; 218: 153
- 562 Li Y.-Y, Zhang X.-Q, Dong Z.-R, Shen W.-Y, Chen G, Gao J.-X. Org. Lett. 2006; 8: 5565
- 563 Zhang X.-Q, Li Y.-Y, Zhang H, Gao J.-X. Tetrahedron: Asymmetry 2007; 18: 2049
- 564 Shen W.-Y, Li Y.-Y, Dong Z.-R, Gao J.-X. Synthesis 2009; 2413
- 565 Xu Y, Docherty GF, Woodward G, Wills M. Tetrahedron: Asymmetry 2006; 17: 2925
- 566 Clarke ML, Díaz-Valenzuela MB, Slawin AM. Z. Organometallics 2007; 26: 16
- 567 Canivet J, Süss-Fink G. Green Chem. 2007; 9: 391
- 568 Sui-Seng C, Freutel F, Lough AJ, Morris RH. Angew. Chem. Int. Ed. 2008; 47: 940
- 569 Shirai SY, Nara H, Kayaki Y, Ikariya T. Organometallics 2009; 28: 802
- 570 Yu S, Shen W, Li Y, Dong Z, Xu Y, Li Q, Zhang J, Gao J. Adv. Synth. Catal. 2012; 354: 818
- 571 Patchett R, Magpantay I, Saudan L, Schotes C, Mezzetti A, Santoro F. Angew. Chem. Int. Ed. 2013; 52: 10352
- 572 Bigler R, Huber R, Mezzetti A. Synlett 2016; 27: 831
- 573 Bigler R, Huber R, Mezzetti A. Angew. Chem. Int. Ed. 2015; 54: 5171
- 574 Bigler R, Mezzetti A. Org. Process Res. Dev. 2016; 20: 253
- 575 Bigler R, Mezzetti A. Org. Lett. 2014; 16: 6460
- 576 Bigler R, Otth E, Mezzetti A. Organometallics 2014; 33: 4086
- 577 De Luca L, Passera A, Mezzetti A. J. Am. Chem. Soc. 2019; 141: 2545
- 578 Mezzetti A. Isr. J. Chem. 2017; 57: 1090
- 579 Li Y, Yu S, Wu X, Xiao J, Shen W, Dong Z, Gao J. J. Am. Chem. Soc. 2014; 136: 4031
- 580 Ling F, Nian S, Chen J, Luo W, Wang Z, Lv Y, Zhong W. J. Org. Chem. 2018; 83: 10749
- 581 Ling F, Hou H, Chen J, Nian S, Yi X, Wang Z, Song D, Zhong W. Org. Lett. 2019; 21: 3937
- 582 Van Putten R, Filonenko GA, Gonzalez de Castro A, Liu C, Weber M, Müller C, Lefort L, Pidko E. Organometallics 2019; 38: 3187
- 583 Endean RT, Rasu L, Bergens SH. ACS Catal. 2019; 9: 6111
- 584 De Luca L, Mezzetti A. Angew. Chem. Int. Ed. 2017; 56: 11949
- 585 De Luca L, Mezzetti A. J. Org. Chem. 2020; 85: 5807
- 586 Sathish M, Nachtigall FM, Santos LS. Org. Lett. 2022; 24: 7627
- 587 Yamashita Y, Yasukawa T, Yoo WJ, Kitanosono T, Kobayashi S. Chem. Soc. Rev. 2018; 47: 4388
- 588 Trost BM, Brindle CS. Chem. Soc. Rev. 2010; 39: 1600
- 589 Denmark SE, Winter SB. D, Su X, Wong K.-T. J. Am. Chem. Soc. 1996; 118: 7404
- 590 Calter MA, Orr RK. Tetrahedron Lett. 2003; 44: 5699
- 591 Shimada Y, Matsuoka Y, Irie R, Katsuki T. Synlett 2004; 57
- 592 Chen D, Timmons C, Liu J, Headley A, Li G. Eur. J. Org. Chem. 2004; 2004: 3330
- 593 Chen D, Guo L, Kotti SR. S. S, Li G. Tetrahedron: Asymmetry 2005; 16: 1757
- 594 Chen J.-R, Lu H.-H, Li X.-Y, Cheng L, Wan J, Xiao W.-J. Org. Lett. 2005; 7: 4543
- 595 Huang W.-P, Chen J.-R, Li X.-Y, Cao Y.-J, Xiao W.-J. Can. J. Chem. 2007; 85: 208
- 596 Choudary BM, Chakrapani L, Ramani T, Kumar KV, Kantam ML. Tetrahedron 2006; 62: 9571
- 597 Chen J.-R, Li X.-Y, Xing X.-N, Xiao W.-J. J. Org. Chem. 2006; 71: 8198
- 598 Kucherenko AS, Siyutkin DE, Muraviev VO, Struchkova MI, Zlotin SG. Mendeleev Commun. 2007; 17: 277
- 599 Luo S, Xu H, Li J, Zhang L, Cheng J.-P. J. Am. Chem. Soc. 2007; 129: 3074
- 600 Luo S, Xu H, Zhang L,