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Volumn 24, Issue 8, 2013, Pages 505-514

Organocatalytic asymmetric addition of aliphatic thiols to nitro olefins and nitrodienes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; NITRO DERIVATIVE; PYRROLIDINE DERIVATIVE; THIOL DERIVATIVE; THIOUREA DERIVATIVE;

EID: 84876382730     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2013.03.007     Document Type: Article
Times cited : (26)

References (82)
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    • for Cinchona alkaloid based urea and thiourea catalysts, see
    • for Cinchona alkaloid based urea and thiourea catalysts, see: S.J. Connon Chem. Comm. 2008 2499
    • (2008) Chem. Comm. , pp. 2499
    • Connon, S.J.1
  • 33
    • 49649104027 scopus 로고    scopus 로고
    • For selected examples of the highly enantioselective addition of aliphatic thiols to Michael acceptors, see
    • For selected examples of the highly enantioselective addition of aliphatic thiols to Michael acceptors, see: D. Leow, S. Lin, S.K. Chittimalla, X. Fu, and C.-H. Tan Angew. Chem., Int. Ed. 47 2008 5641
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 5641
    • Leow, D.1    Lin, S.2    Chittimalla, S.K.3    Fu, X.4    Tan, C.-H.5
  • 49
    • 4244018761 scopus 로고
    • For reviews concerning addition to extended Michael acceptors, see
    • For reviews concerning addition to extended Michael acceptors, see: J.W. Ralls Chem. Rev. 59 1959 329
    • (1959) Chem. Rev. , vol.59 , pp. 329
    • Ralls, J.W.1
  • 57
    • 33947274570 scopus 로고    scopus 로고
    • 1,4-Additions seem to be favoured over the expected 1,6-additions for carbon and phosphorus nucleophiles. For examples of such regioslectivity, see
    • 1,4-Additions seem to be favoured over the expected 1,6-additions for carbon and phosphorus nucleophiles. For examples of such regioslectivity, see: S.-Y. Park, H. Morimoto, S. Matsunaga, and M. Shibasaki Tetrahedron Lett. 48 2007 2815
    • (2007) Tetrahedron Lett. , vol.48 , pp. 2815
    • Park, S.-Y.1    Morimoto, H.2    Matsunaga, S.3    Shibasaki, M.4
  • 69
    • 84870359712 scopus 로고    scopus 로고
    • However, highly regioselective 1,6- and 1,8-additions of azlactones to di- and trienyl N-acylpyrroles were reported
    • However, highly regioselective 1,6- and 1,8-additions of azlactones to di- and trienyl N-acylpyrroles were reported: D. Uraguchi, K. Yoshioka, Y. Ueki, and T. Ooi J. Am. Chem. Soc. 134 2012 19370
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 19370
    • Uraguchi, D.1    Yoshioka, K.2    Ueki, Y.3    Ooi, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.