Synthesis 2022; 54(21): 4773-4783
DOI: 10.1055/a-1801-2595
special topic
Asymmetric C–H Functionalization

Enantioselective Cobalt-Catalyzed C–H Functionalization

Weiwei Xu
a   State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin 300071, P. R. of China
,
Mengchun Ye
a   State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin 300071, P. R. of China
b   Haihe Laboratory of Sustainable Chemical Transformations, Tianjin 300192, P. R. of China
› Author Affiliations
We thank the National Natural Science Foundation of China (21871145 and 22188101), Tianjin Applied Basic Research Project and Cutting-Edge Technology Research Plan (19JCZDJC37900), the Haihe Laboratory of Sustainable Chemical Transformations, and Frontiers Science Center for New Organic Matter (63181206) for financial support.


Abstract

Co-catalyzed C–H functionalization has received great attention due to the high earth abundance, low biotoxicity, and unique reactivity of cobalt; enantioselective control of these reactions has been a formidable challenge. Various efficient strategies have recently been developed for enantioselective Co-catalyzed C–H functionalization, but there is no topical review of this field. Herein, we give a detailed summary of this rapidly growing field, highlighting critical progress, current challenges, and future trends.

1 Introduction

2 Enantioselective C–H Functionalization via Low-Valent Co Catalysis

2.1 Chiral Diphosphines for Enantioselective Control

2.2 Chiral Monophosphines or N-Heterocyclic Carbenes for Enantioselective Control

3 Enantioselective C–H Functionalization via High-Valent Co Catalysis

3.1 Chiral Acids for Enantioselective Control

3.2 Chiral Cp Ligands for Enantioselective Control

4 Conclusions and Outlook



Publication History

Received: 17 February 2022

Accepted after revision: 17 March 2022

Accepted Manuscript online:
17 March 2022

Article published online:
12 May 2022

© 2022. Thieme. All rights reserved

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Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References


    • For selected reviews on transition-metal-catalyzed C–H functionalization, see:
    • 1a Ackermann L, Vicente R, Kapdi AR. Angew. Chem. Int. Ed. 2009; 48: 9792
    • 1b Colby DA, Bergman RG, Ellman JA. Chem. Rev. 2010; 110: 624
    • 1c Lyons TW, Sanford MS. Chem. Rev. 2010; 110: 1147
    • 1d Gutekunst WR, Baran PS. Chem. Soc. Rev. 2011; 40: 1976
    • 1e Yeung CS, Dong VM. Chem. Rev. 2011; 111: 1215
    • 1f McMurray L, O’Hara F, Gaunt MJ. Chem. Soc. Rev. 2011; 40: 1885
    • 1g Yamaguchi J, Yamaguchi AD, Itami K. Angew. Chem. Int. Ed. 2012; 51: 8960
    • 1h Engle KM, Mei TS, Wasa M, Yu JQ. Acc. Chem. Res. 2012; 45: 788
    • 1i Wencel-Delord J, Glorius F. Nat. Chem. 2013; 5: 369
    • 1j Rouquet G, Chatani N. Angew. Chem. Int. Ed. 2013; 52: 11726
    • 1k Daugulis O, Roane J, Tran LD. Acc. Chem. Res. 2015; 48: 1053
    • 1l Chen Z, Wang B, Zhang J, Yu W, Liu Z, Zhang Y. Org. Chem. Front. 2015; 2: 1107
    • 1m Tao P, Jia Y. Sci. China Chem. 2016; 59: 1109
    • 1n Hartwig JF, Larsen MA. ACS Cent. Sci. 2016; 2: 281
    • 1o Gensch T, Hopkinson MN, Glorius F, Wencel-Delord J. Chem. Soc. Rev. 2016; 45: 2900
    • 1p Leitch JA, Frost CG. Chem. Soc. Rev. 2017; 46: 7145
    • 1q Newton CG, Wang SG, Oliveira CC, Cramer N. Chem. Rev. 2017; 117: 8908
    • 1r Hummel JR, Boerth JA, Ellman JA. Chem. Rev. 2017; 117: 9163
    • 1s Shang R, Ilies L, Nakamura E. Chem. Rev. 2017; 117: 9086
    • 1t Gandeepan P, Ackermann L. Chem 2018; 4: 199
    • 1u Li JF, Luan YX, Ye M. Sci. China Chem. 2021; 64: 1923

      For selected reviews on 3d-transition-metal-catalyzed C–H functionalization, see:
    • 2a Kulkarni AA, Daugulis O. Synthesis 2009; 4087
    • 2b Nakao Y. Chem. Rec. 2011; 11: 242
    • 2c Su B, Cao ZC, Shi Z.-J. Acc. Chem. Res. 2015; 48: 886
    • 2d Miao J, Ge H. Eur. J. Org. Chem. 2015; 7859
    • 2e Xu ZY, Yu HZ, Fu Y. Sci. China Chem. 2017; 60: 165
    • 2f Pototschnig G, Maulide N, Schnuerch M. Chem. Eur. J. 2017; 23: 9206
    • 2g Rajesh N, Barsu N, Sundararaju B. Tetrahedron Lett. 2018; 59: 862
    • 2h Loup J, Dhawa U, Pesciaioli F, Wencel-Delord JW, Ackermann L. Angew. Chem. Int. Ed. 2019; 58: 12803
    • 2i Gandeepan P, Müller T, Zell D, Cera G, Warratz S, Ackermann L. Chem. Rev. 2019; 119: 2192
    • 2j Wozniak L, Cramer N. Trends Chem. 2019; 1: 471
    • 2k Bansal S, Shabade AB, Punji B. Adv. Synth. Catal. 2021; 363: 1998
    • 2l Ilies L. Bull. Chem. Soc. Jpn. 2021; 94: 404
  • 3 Murahashi S. J. Am. Chem. Soc. 1955; 77: 6403
  • 4 Gao K, Lee PS, Fujita T, Yoshikai N. J. Am. Chem. Soc. 2010; 132: 12249

    • For selected reviews on Co-catalyzed C–H functionalization, see:
    • 5a Gao K, Yoshikai N. Acc. Chem. Res. 2014; 47: 1208
    • 5b Ackermann L. J. Org. Chem. 2014; 79: 8948
    • 5c Yoshikai N. Bull. Chem. Soc. Jpn. 2014; 87: 843
    • 5d Yoshikai N. ChemCatChem 2015; 7: 732
    • 5e Wei D, Zhu X, Niu JL, Song MP. ChemCatChem 2016; 8: 1242
    • 5f Usman M, Ren ZH, Wang YY, Guan ZH. Synthesis 2017; 49: 1419
    • 5g Wang S, Chen SY, Yu XQ. Chem. Commun. 2017; 53: 3165
    • 5h Yoshino T, Matsunaga S. Adv. Synth. Catal. 2017; 359: 1245
    • 5i Kommagalla Y, Chatani N. Coord. Chem. Rev. 2017; 350: 117
    • 5j Yoshino T, Matsunaga S. Adv. Organomet. Chem. 2017; 68: 197
    • 5k Chirila PG, Whiteoak CJ. Dalton Trans. 2017; 46: 9721
    • 5l Ujwaldev SM, Harry NA, Divakar MA, Anilkumar G. Catal. Sci. Technol. 2018; 8: 5983
    • 5m Yoshino T, Matsunaga S. Asian J. Org. Chem. 2018; 7: 1193
    • 5n Mei RH, Dhawa U, Samatan RC, Ma W, Wencel-Delord J, Ackermann L. ChemSusChem 2020; 13: 3306
    • 5o Liu Y, You T, Wang HX, Tang Z, Zhou CY, Che CM. Chem. Soc. Rev. 2020; 49: 5310
    • 5p Fernández DF, Mascareñas JL, López F. Chem. Soc. Rev. 2020; 49: 7378
    • 5q Lukasevicsa L, Grigorjeva L. Org. Biomol. Chem. 2020; 18: 7460
    • 5r Banjare SK, Nanda T, Pati BV, Biswal P, Ravikumar PC. Chem. Commun. 2021; 57: 3630
    • 5s Sunny S, Karvembua R. Adv. Synth. Catal. 2021; 363: 4309
    • 5t Hamilton A, Whiteoak C. J. Organomet. Chem. 2021; 43: 186
    • 5u Cizikovs A, Lukasevics L, Grigorjeva L. Tetrahedron 2021; 93: 132307
    • 5v Yoshino T, Matsunaga S. ACS Catal. 2021; 11: 6455

      For reviews that summarize enantioselective Co-catalyzed C–H functionalization into subsections, see:
    • 6a Yoshino T, Matsunaga S. Synlett 2019; 30: 1384
    • 6b Mishra AA, Subhedar D, Bhanage BM. Chem. Rec. 2019; 19: 1829
    • 6c Baccalini A, Vergura S, Dolui P, Zanoni G, Maiti D. Org. Biomol. Chem. 2019; 17: 10119
    • 6d Yoshino T, Satake S, Matsunaga S. Chem. Eur. J. 2020; 26: 7346
    • 6e Lukasevics L, Cizikovsa A, Grigorjeva L. Chem. Commun. 2021; 57: 10827
    • 6f Davison RT, Kuker EL, Dong VM. Acc. Chem. Res. 2021; 54: 1236

      For selected reviews on Co-involved photo- or electrocatalysis, see:
    • 7a Sauermann N, Meyer TH, Ackermann L. Chem. Eur. J. 2018; 24: 16209
    • 7b Kojima M, Matsunaga S. Trends Chem. 2020; 2: 410
    • 7c Zhong J, Yu Y, Zhang D, Ye K. Chin. Chem. Lett. 2021; 32: 963
    • 7d Chakraborty P, Mandal R, Paira S, Sundararaju B. Chem. Commun. 2021; 57: 13075

      For recent progress from Zhang group, see:
    • 8a Xie J.-J, Xu P, Zhu Y.-L, Wang J.-Y, Lee W.-CC, Zhang XP. J. Am. Chem. Soc. 2021; 143: 11670
    • 8b Lang K, Li C.-Q, Kim I, Zhang XP. J. Am. Chem. Soc. 2020; 142: 20902
    • 8c Jin L.-M, Xu P, Xie J.-J, Zhang XP. J. Am. Chem. Soc. 2020; 142: 20828
    • 8d Hu Y, Lang K, Li C.-Q, Gill JB, Kim I, Lu H.-J, Fields KB, Marshall MK, Cheng Q.-G, Cui X, Wojtas L, Zhang XP. J. Am. Chem. Soc. 2019; 141: 18160
    • 9a Moselage M, Li J, Ackermann L. ACS Catal. 2016; 6: 498
    • 9b Planas O, Chirila PG, Whiteoak CJ, Ribas X. Adv. Organomet. Chem. 2018; 69: 209

      For selected examples on diphosphine-enabled enantioselective Co-catalyzed transformation of π-unsaturated compounds, see:
    • 10a Kundu K, McCullagh JV, Morehead AT. J. Am. Chem. Soc. 2005; 127: 16042
    • 10b Phan DH. T, Kim B, Dong VM. J. Am. Chem. Soc. 2009; 131: 15608
    • 10c Phan DH, Kou KG. M, Dong VM. J. Am. Chem. Soc. 2010; 132: 16354
    • 10d Sharma RK, RajanBabu TV. J. Am. Chem. Soc. 2010; 132: 3295
    • 10e Wei CH, Mannathan S, Cheng CH. J. Am. Chem. Soc. 2011; 133: 6942
    • 10f Sawano T, Ashouri A, Nishimura T, Hayashi T. J. Am. Chem. Soc. 2012; 134: 18936
    • 10g Wei CH, Mannathan S, Cheng CH. Angew. Chem. Int. Ed. 2012; 51: 10592
    • 10h Gandeepan P, Cheng CH. Acc. Chem. Res. 2015; 48: 1194
  • 11 Yang J, Yoshikai N. J. Am. Chem. Soc. 2014; 136: 16748
    • 12a Yang J, Rerat A, Lim YJ, Gosmini C, Yoshikai N. Angew. Chem. Int. Ed. 2017; 56: 2449

    • For relevant examples on asymmetric Rh-catalyzed versions, see:
    • 12b James BR, Young CG. J. Chem. Soc., Chem. Commun. 1983; 1215
    • 12c James BR, Young CG. J. Organomet. Chem. 1985; 285: 321
    • 12d Wu X, Funakoshi K, Sakai K. Tetrahedron Lett. 1992; 33: 6331
    • 12e Barnhart RW, Wang XQ, Noheda P, Bergens SH, Whelan J, Bosnich B. J. Am. Chem. Soc. 1994; 116: 1821
    • 12f Barnhart RW, McMorran DA, Bosnich B. Chem. Commun. 1997; 589
    • 12g Tanaka M, Sakai K, Suemune H. Curr. Org. Chem. 2003; 7: 353
    • 12h Hoffman TJ, Carreira EM. Angew. Chem. Int. Ed. 2011; 50: 10670
    • 13a Kim DK, Riedel J, Kim RS, Dong VM. J. Am. Chem. Soc. 2017; 139: 10208

    • For Rh-catalyzed formation of four-membered cyclobutanones, see:
    • 13b Yip SY. Y, Aïssa C. Angew. Chem. Int. Ed. 2015; 54: 6870
    • 13c Tanaka K, Fu GC. J. Am. Chem. Soc. 2003; 125: 8078
    • 14a Whyte A, Bajohr J, Torelli A, Lautens M. Angew. Chem. Int. Ed. 2020; 59: 16409
    • 14b Whyte A, Torelli A, Mirabi B, Prieto L, Rodríguez JE, Lautens M. J. Am. Chem. Soc. 2020; 142: 9510

    • For Rh-catalyzed version, see:
    • 14c Santhoshkumar R, Mannathan S, Cheng CH. J. Am. Chem. Soc. 2015; 137: 16116
  • 15 Lee PS, Yoshikai N. Org. Lett. 2015; 17: 22
  • 16 Jacob N, Zaid Y, Oliveira JC. A, Ackermann L, Wencel-Delord J. J. Am. Chem. Soc. 2022; 144: 798
    • 17a Nguyen QH, Guo SM, Royal T, Baudoin O, Cramer N. J. Am. Chem. Soc. 2020; 142: 2161
    • 17b Woźniak Ł, Cramer N. Angew. Chem. Int. Ed. 2021; 60: 18532
  • 18 Zell D, Bursch M, Mgller V, Grimme S, Ackermann L. Angew. Chem. Int. Ed. 2017; 56: 10378
  • 19 Pesciaioli F, Dhawa U, Oliveira JC. A, Yin R, John M, Ackermann L. Angew. Chem. Int. Ed. 2018; 57: 15425

    • For selected reviews on C(sp3)–H activation, see:
    • 20a Baudoin O. Chem. Soc. Rev. 2011; 40: 4902
    • 20b Dastbaravardeh N, Christakakou M, Haider M, Schnerch M. Synthesis 2014; 46: 1421
    • 20c He J, Wasa M, Chan KS. L, Shao Q, Yu JQ. Chem. Rev. 2017; 117: 8754
    • 20d Chu JC. K, Rovis T. Angew. Chem. Int. Ed. 2018; 57: 62
    • 20e Karimov RR, Hartwig JF. Angew. Chem. Int. Ed. 2018; 57: 4234
    • 20f Xu Y, Dong G. Chem. Sci. 2018; 9: 1424
  • 21 Tan PW, Mak AM, Sullivan MB, Dixon DJ, Seayad J. Angew. Chem. Int. Ed. 2017; 56: 16550
  • 22 Fukagawa S, Kato Y, Tanaka R, Kojima M, Yoshino T, Matsunaga S. Angew. Chem. Int. Ed. 2019; 58: 1153
  • 23 Kurihara T, Kojima M, Yoshino T, Matsunaga S. Asian J. Org. Chem. 2020; 9: 368
  • 24 Zhang Z, Han S, Tang M, Ackermann L, Li J. Org. Lett. 2017; 19: 3315
  • 25 Sekine D, Ikeda K, Fukagawa S, Kojima M, Yoshino T, Matsunaga S. Organometallics 2019; 38: 3921
  • 26 Liu YH, Li PX, Yao QJ, Zhang ZZ, Huang DY, Le MD, Song H, Liu L, Shi BF. Org. Lett. 2019; 21: 1895
  • 27 Liu YH, Xie PP, Liu L, Fan J, Zhang ZZ, Hong X, Shi BF. J. Am. Chem. Soc. 2021; 143: 19112
  • 28 Yuan WK, Shi BF. Angew. Chem. Int. Ed. 2021; 60: 23187
  • 29 Yoshino T, Ikemoto H, Matsunaga S, Kanai M. Angew. Chem. Int. Ed. 2013; 52: 2207
    • 30a Hyster TK, Knorr L, Ward TR, Rovis T. Science 2012; 338: 500
    • 30b Ye B, Cramer N. Acc. Chem. Res. 2015; 48: 1308
    • 30c Newton CG, Kossler D, Cramer N. J. Am. Chem. Soc. 2016; 138: 3935
    • 30d Zheng J, Cui WJ, Zheng C, You SL. J. Am. Chem. Soc. 2016; 138: 5242
    • 30e Jia ZJ, Merten C, Gontla R, Daniliuc CG, Antonchick AP, Waldmann H. Angew. Chem. Int. Ed. 2017; 56: 2429
    • 30f Smits G, Audic B, Wodrich MD, Corminboeuf C, Cramer N. Chem. Sci. 2017; 8: 7174
    • 30g Sun Y, Cramer N. Chem. Sci. 2018; 9: 2981
    • 30h Trifonova EA, Ankudinov NM, Mikhaylov AA, Chusov DA, Nelyubina YV, Perekalin DS. Angew. Chem. Int. Ed. 2018; 57: 7714
    • 30i Wang SG, Park SH, Cramer N. Angew. Chem. Int. Ed. 2018; 57: 5459
  • 31 Ozols K, Jang YS, Cramer N. J. Am. Chem. Soc. 2019; 141: 5675
  • 32 Ozols K, Onodera S, Woźniak Ł, Cramer N. Angew. Chem. Int. Ed. 2021; 60: 655
  • 33 Herraiz AG, Cramer N. ACS Catal. 2021; 11: 11938
  • 34 Boerth JA, Hummel JR, Ellman JA. Angew. Chem. Int. Ed. 2016; 55: 12650