메뉴 건너뛰기




Volumn 2015, Issue 3, 2015, Pages 525-533

Preparation and catalytic activity of BINOL-derived silanediols

Author keywords

Anion recognition; Asymmetric catalysis; Hydrogen bonds; Organocatalysis; Silanediols

Indexed keywords


EID: 84921048184     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201403441     Document Type: Article
Times cited : (66)

References (74)
  • 11
    • 80051965578 scopus 로고    scopus 로고
    • Angew. Chem. 1998, 110, 845-847;
    • (1998) Angew. Chem. , vol.110 , pp. 845-847
  • 35
    • 84890576508 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 11531-11534.
    • (2013) Angew. Chem. , vol.125 , pp. 11531-11534
  • 39
    • 33746322013 scopus 로고    scopus 로고
    • Angew. Chem. 2006, 118, 1550-1573;
    • (2006) Angew. Chem. , vol.118 , pp. 1550-1573
  • 43
    • 84875425517 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 558-588.
    • (2013) Angew. Chem. , vol.125 , pp. 558-588
  • 45
    • 77951758941 scopus 로고    scopus 로고
    • For information on (thio) urea catalysis, see: a) Y. Takemoto, Chem. Pharm. Bull. 2010, 58, 593-601;
    • (2010) Chem. Pharm. Bull. , vol.58 , pp. 593-601
    • Takemoto, Y.1
  • 49
    • 69249092514 scopus 로고    scopus 로고
    • For recent reviews on Brønsted acid catalysis, see: a) S. You, Q. Cai, M. Zeng, Chem. Soc. Rev. 2009, 38, 2190-2201;
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2190-2201
    • You, S.1    Cai, Q.2    Zeng, M.3
  • 51
    • 38349189109 scopus 로고    scopus 로고
    • T. Akiyama, Chem. Rev. 2007, 107, 5744-5758;
    • (2007) Chem. Rev. , vol.107 , pp. 5744-5758
    • Akiyama, T.1
  • 53
    • 41849139741 scopus 로고    scopus 로고
    • Select, impressive features of BINOL in catalysis have been reviewed, see: a) J. M. Brunel, Chem. Rev. 2007, 107, Pr1-Pr45;
    • (2007) Chem. Rev. , vol.107 , pp. Pr1-Pr45
    • Brunel, J.M.1
  • 55
  • 62
    • 0000950741 scopus 로고    scopus 로고
    • See Supporting Information for details. For a general reference for the resolution of substituted BINOL backbones, see: H.-F. Chow, C.-W. Wan, M.-K. Ng, J. Org. Chem. 1996, 61, 8712-8714.
    • (1996) J. Org. Chem. , vol.61 , pp. 8712-8714
    • Chow, H.-F.1    Wan, C.-W.2    Ng, M.-K.3
  • 64
    • 33746319084 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 6858-6862.
    • (2005) Angew. Chem. , vol.117 , pp. 6858-6862
  • 68
    • 34347212512 scopus 로고    scopus 로고
    • for systematic studies probing the effect of HBD acidity on HBD catalyst performance, see: d) K. H. Jensen, M. S. Sigman, Angew. Chem. Int. Ed. 2007, 46, 4748-4750;
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4748-4750
    • Jensen, K.H.1    Sigman, M.S.2
  • 69
    • 38349077273 scopus 로고    scopus 로고
    • Angew. Chem. 2007, 119, 4832-4834;
    • (2007) Angew. Chem. , vol.119 , pp. 4832-4834
  • 73
    • 84900852336 scopus 로고    scopus 로고
    • for computational studies on chiral Brønsted acids and HBDs, including chiral silanediols, see: c) C. Yang, X.-S. Xue, X. Li, J.-P. Cheng, J. Org. Chem. 2014, 79, 4340-4351.
    • (2014) J. Org. Chem. , vol.79 , pp. 4340-4351
    • Yang, C.1    Xue, X.-S.2    Li, X.3    Cheng, J.-P.4
  • 74
    • 84921038219 scopus 로고    scopus 로고
    • CCDC-947138, -947139, -1023331, and -1023332 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.