Synlett 2012; 23(11): 1575-1589
DOI: 10.1055/s-0031-129068
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© Georg Thieme Verlag Stuttgart · New York

Bio-inspired Chiral Primary Amine Catalysis

Long Zhang
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. of China, Fax: +86(10)62554449   eMail: luosz@iccas.ac.cn
,
Sanzhong Luo*
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. of China, Fax: +86(10)62554449   eMail: luosz@iccas.ac.cn
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Publikationsverlauf

Received: 20. Januar 2012

Accepted after revision: 05. März 2012

Publikationsdatum:
11. Juni 2012 (online)


Abstract

The search for new catalysts with superior performance and broad applicability remains a central theme in asymmetric organocatalysis. Inspired by Nature as well as by numerous previous efforts, we have developed chiral primary–tertiary diamines as both functional and mechanistic enzyme mimics, showing unprecedented scope in enamine-aldol reactions and significant potential in the reactions of acroleins. Our endeavors focusing on this type of catalysts are summarized in this account.

1 Introduction

2 General Features of Primary–Tertiary Vicinal Diamine/TfOH; Multifunctional Catalysis

3 Asymmetric Supramolecular Primary Amine Catalysis; Roles of the Hydrophobic Cavity

4 Asymmetric Direct Aldol Reaction of Aliphatic Ketones

5 Asymmetric Direct Cross-Aldol Reaction of Aldehydes

6 Asymmetric Retro-Aldol and Transfer-Aldol Reactions

7 Iminium Catalysis with Chiral Primary–Tertiary Diamines

8 Bifunctional Catalysis of Primary–Tertiary Diamines in the Baylis–Hillman Reaction

9 Conclusion, Remarks, and Outlook

 
  • References

  • 1 In Privileged Chiral Ligands and Catalysts . Zhou Q.-L. Wiley-VCH; Weinheim: 2011
    • 2a Berkessel A, Gröger H. Asymmetric Organocatalysis . Wiley-VCH; Weinheim: 2005
    • 2b For recent reviews on aminocatalysis, see: Mukherjee S, Yang JW, Hoffmann S, List B. Chem. Rev. 2007; 107: 5471
    • 2c See also: Erkkila A, Majander I, Pihko PM. Chem. Rev. 2007; 107: 5416
  • 3 For our other efforts along this line, see: Luo S, Zhang L, Cheng J.-P. Chem. Asian J. 2009; 4: 1184
    • 5a Gefflaut T, Blonksi C, Perie J, Willson M. Prog. Biophys. Molec. Biol. 1995; 63: 301
    • 5b Gijsen HJ. M, Qiao L, Fitz W, Wong C.-H. Chem. Rev. 1996; 96: 443
    • 6a Harada N, Sugioka T, Uda H, Kuriki T. Synthesis 1990; 53
    • 6b Clemente FR, Houk KN. J. Am. Chem. Soc. 2005; 127: 11294 ; and references therein
    • 6c Mander LN, Turner JV. Tetrahedron Lett. 1981; 22: 3683
    • 6d Hagiwara H, Uda H. J. Org. Chem. 1988; 53: 2308
    • 7a Ibrahem I, Zou W, Engqvist M, Xu Y, Córdova A. Chem. Eur. J. 2005; 11: 7024
    • 7b Córdova A, Zou WB, Ibrahem I, Reyes E, Engqvist M, Liao WW. Chem. Commun. 2005; 3586
  • 8 Tsogoeva SB, Wei S. Chem. Commun. 2006; 1451
  • 9 Huang H, Jacobsen EN. J. Am. Chem. Soc. 2006; 128: 7170
  • 10 Ramasastry SS. V, Zhang H, Tanaka F, Barbas CF. III. J. Am. Chem. Soc. 2007; 129: 288
    • 11a Xu X.-Y, Wang Y.-Z, Gong L.-Z. Org. Lett. 2007; 9: 4247
    • 11b Li J, Yang Z, Wang Z, Wang F, Chen X, Liu X, Feng X.-M. J. Am. Chem. Soc. 2008; 130: 5654
    • 11c Wu X, Ma Z, Ye Z, Qian S, Zhao G. Adv. Synth. Catal. 2009; 351: 158
    • 12a Westheimer FH. Tetrahedron 1995; 51: 3
    • 12b Heine A, DeSantis G, Luz JG, Mitchell M, Wong C.-H, Wilson IA. Science 2001; 294: 369
    • 13a Barbas CF. III, Heine A, Zhong G, Hoffmann T, Gramatikova S, Bjornestedt R, List B, Anderson J, Stura EA, Wilson IA, Lerner RA. Science 1997; 278: 2085
    • 13b Ho M.-C, Menetret J.-F, Tsuruta H, Allen KN. Nature 2009; 459: 393
  • 14 Hine J. Acc. Chem. Res. 1978; 11: 1
  • 15 For a recent discussion, see: Saito S, Yamamoto H. Acc. Chem. Res. 2004; 37: 570
  • 16 Luo S, Xu H, Li J, Zhang L, Cheng J.-P. J. Am. Chem. Soc. 2007; 129: 3074
  • 17 Li J, Xu H, Xue X, Luo S, Cheng J.-P unpublished results
  • 18 Hu S, Li J, Xiang J, Pan J, Luo S, Cheng J.-P. J. Am. Chem. Soc. 2010; 132: 7216

    • For reviews on enzyme mimics based on cyclodextrin, see:
    • 19a Breslow R, Dong SD. Chem. Rev. 1998; 98: 1997
    • 19b Rekharsky MV, Inoue Y. Chem. Rev. 1998; 98: 1875
    • 20a Breslow R, Graff A. J. Am. Chem. Soc. 1993; 115: 10988
    • 20b Desper JM, Breslow R. J. Am. Chem. Soc. 1994; 116: 12081
    • 21a Brogan AP, Dickerson TJ, Janda KD. Angew. Chem. Int. Ed. 2006; 45: 8100
    • 21b Hayashi Y. Angew. Chem. Int. Ed. 2006; 45: 8103
    • 21c Blackmond DG, Armstrong A, Coombe V, Wells A. Angew. Chem. Int. Ed. 2007; 46: 3798
  • 22 Trost BM, Brindle CS. Chem. Soc. Rev. 2010; 39: 1600
  • 23 Li J, Luo S, Cheng J.-P. J. Org. Chem. 2009; 74: 1747
    • 24a Enders D, Voith M, Lenzen A. Angew. Chem. Int. Ed. 2005; 44: 1304
    • 24b Wong C.-H, Machajewski TD. Angew. Chem. Int. Ed. 2000; 39: 1352
    • 25a For a selected example, see: Enders D, Grondal C. Angew. Chem. Int. Ed. 2005; 44: 1210
    • 25b For syn-selective aldol reaction of protected dihydroxyacetones, see: Utsumi N, Imai M, Tanaka F, Ramasastry S.s.V, Barbas CF. III. Org. Lett. 2007; 9: 3445

      For direct aldol reaction of free DHA with low stereoselectivity or racemic products, see:
    • 26a Córdova A, Notz W, Barbas CF. III. Chem. Commun. 2002; 3024
    • 26b Market M, Mulzer M, Schetter B, Mahrwald R. J. Am. Chem. Soc. 2007; 129: 7258
    • 26c Kofoed J, Darbre T, Reymond J.-L. Chem. Commun. 2006; 1482
    • 26d For a successful syn-aldol reaction of free dihydroxyacetone, see: Ramasastry SS. V, Albertshofer K, Utsumi N, Tanaka F, Barbas CF. III. Angew. Chem. Int. Ed. 2007; 46: 5572
  • 27 Luo S, Xu H, Zhang L, Li J, Cheng J.-P. Org. Lett. 2008; 10: 653
    • 28a Angata T, Varki A. Chem. Rev. 2002; 102: 439
    • 28b Wong C.-H In Enzymes in Synthetic Organic Chemistry . Wong C.-H, Whitesides GM. Elsevier; Oxford: 1994: 215-219
    • 29a Enders D, Gasperi T. Chem. Commun. 2007; 88
    • 29b Schetter B, Mahrwald R. Angew. Chem. Int. Ed. 2006; 45: 7506
  • 30 Luo S, Xu H, Chen L, Cheng J.-P. Org. Lett. 2008; 10: 1774
  • 31 Denmark SE, Heemstra JR, Beutner GL. Angew. Chem. Int. Ed. 2005; 44: 4682
  • 32 Luo S, Qiao Y, Zhang L, Li J, Li X, Cheng J.-P. J. Org. Chem. 2009; 74: 9521
  • 33 Qiao Y. Ph.D. Thesis. Institute of Chemistry, The Chinese Academy of Sciences; P. R. of China: 2011
    • 34a Eder U, Sauer G, Wiechert R. Angew. Chem. Int. Ed. Engl. 1971; 10: 496 Angew. Chem. 1971; 83 492
    • 34b Hajos ZG, Parrish DR. J. Org. Chem. 1973; 38: 3239
    • 34c Hajos ZG, Parrish DR. J. Org. Chem. 1974; 39: 1615
  • 35 Bradshaw B, Etxebarria-Jardi G, Bonjoch J, Viozquez SF, Guillena G, Najera C. Adv. Synth. Catal. 2009; 351: 2482
  • 36 Zhou P, Zhang L, Luo S, Cheng J.-P. J. Org. Chem. 2012; 77: 2526

    • For a review, see:
    • 37a Zhang L, Luo S, Cheng J.-P. Catal. Sci. Technol. 2011; 1: 507
    • 37b Luo S, Li J, Zhang L, Xu H, Cheng J.-P. Chem. Eur. J. 2008; 14: 1273
  • 38 Luo S, Zheng X, Cheng J.-P. Chem. Commun. 2008; 5719
    • 40a Kano T, Yamaguchi Y, Tanaka Y, Maruoka K. Angew. Chem. Int. Ed. 2007; 46: 1738
    • 40b Kano T, Yamaguchi Y, Maruoka K. Chem. Eur. J. 2009; 15: 6678
  • 41 Li J, Fu N, Li X, Luo S, Cheng J.-P. J. Org. Chem. 2010; 75: 4501
  • 42 For reviews on organocatalytic reactions with acetaldehyde, see: Alcaide B, Almendros P. Angew. Chem. Int. Ed. 2008; 47: 4632
  • 43 For an example, see: Hayashi Y, Itoh T, Aratake S, Ishikawa H. Angew. Chem. Int. Ed. 2008; 47: 2082
  • 44 Hu S, Zhang L, Li J, Luo S, Cheng J.-P. Eur. J. Org. Chem. 2011; 3347
    • 45a Flanagan ME, Jacobsen JR, Sweet E, Schultz PG. J. Am. Chem. Soc. 1996; 118: 6078
    • 45b Zhong GF, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas CF. III. Angew. Chem. Int. Ed. 1998; 37: 2481
    • 46a Tosaki SY, Hara K, Gnanadesikan V, Morimoto H, Harada S, Sugita M, Yamagiwa N, Matsunaga S, Shibasaki M. J. Am. Chem. Soc. 2006; 128: 11776
    • 46b Hara K, Tosaki SY, Gnanadesikan V, Morimoto H, Harada S, Sugita M, Yamagiwa N, Matsunaga S, Shibasaki M. Tetrahedron 2009; 65: 5030
  • 47 Luo S, Zhou P, Li J, Cheng J.-P. Chem. Eur. J. 2010; 16: 4457
  • 48 Zhou P, Luo S, Cheng J.-P. Org. Biomol. Chem. 2011; 9: 1784
    • 49a Ishihara K, Nakano K. J. Am. Chem. Soc. 2005; 127: 10504
    • 49b Sakakura A, Suzuki K, Nakano K, Ishihara K. Org. Lett. 2006; 8: 2229
    • 49c Sakakura A, Suzuki K, Ishihara K. Adv. Synth. Catal. 2006; 348: 2457
    • 49d Ishihara K, Nakano K, Akakura M. Org. Lett. 2008; 10: 2893
    • 49e Ishihara K, Nakano K. J. Am. Chem. Soc. 2007; 129: 8930
  • 50 Kano T, Tanaka Y, Osawa K, Yurino T, Maruoka K. Chem. Commun. 2009; 1956
  • 51 Lifchits O, Reisinger CM, List B. J. Am. Chem. Soc. 2010; 132: 10227
  • 52 Erkkila A, Pihko PM, Clark M.-R. Adv. Synth. Catal. 2007; 349: 802
  • 53 Li J, Li X, Zhou P, Zhang L, Luo S, Cheng J.-P. Eur. J. Org. Chem. 2009; 4486
  • 54 Li J, Fu N, Zhang L, Zhou P, Luo S, Cheng J.-P. Eur. J. Org. Chem. 2010; 6840
  • 55 Bondzic BP, Urushima T, Ishikawa H, Hayashi Y. Org. Lett. 2010; 12: 5434
  • 56 Fu N, Zhang L, Li J, Luo S, Cheng J.-P. Angew. Chem. Int. Ed. 2011; 50: 11451
  • 57 Mohr JT, Hong AY, Stoltz BM. Nat. Chem. 2009; 1: 359
  • 58 Zhang L, Luo SZ, Chen LJ, Li J, Cheng J.-P. Sci. China, Ser. B: Chem. 2009; 52: 1300
  • 59 Gruttadauria M, Giacalone F, Paolo Lo Meo P, Marculescu AM, Riela S, Noto R. Eur. J. Org. Chem. 2008; 1589