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Volumn 9, Issue 19, 2007, Pages 3717-3720

Highly enantioselective Michael additions in water catalyzed by a PS-supported pyrrolidine

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EID: 34848859862     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071366k     Document Type: Article
Times cited : (200)

References (41)
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    • For reviews on immobilized organocatalysts, see: a
    • For reviews on immobilized organocatalysts, see: (a) Benaglia, M.; Puglisi, A.; Cozzi, F. Chem. Rev. 2003, 103, 3401.
    • (2003) Chem. Rev , vol.103 , pp. 3401
    • Benaglia, M.1    Puglisi, A.2    Cozzi, F.3
  • 11
    • 34848920359 scopus 로고    scopus 로고
    • Lebl, M, Houghten, R. A, Eds, American Peptide Society and Kluwer Academic Press: San Diego
    • (a) Tornøe, C. W.; Meldal, M. In Proc. Second Intl. and Seventeenth Amer. Peptide Soc. Symp.; Lebl, M., Houghten, R. A., Eds.; American Peptide Society and Kluwer Academic Press: San Diego, 2001; pp 263-264.
    • (2001) Proc. Second Intl. and Seventeenth Amer. Peptide Soc. Symp , pp. 263-264
    • Tornøe, C.W.1    Meldal, M.2
  • 17
    • 20744459179 scopus 로고    scopus 로고
    • For assessments on the suitability of click chemistry as a supporting strategy in metal catalysis, see: a
    • For assessments on the suitability of click chemistry as a supporting strategy in metal catalysis, see: (a) Gissibi, A.; Finn, M. G.; Reiser, O. Org. Lett. 2005, 7, 2325-2328.
    • (2005) Org. Lett , vol.7 , pp. 2325-2328
    • Gissibi, A.1    Finn, M.G.2    Reiser, O.3
  • 29
    • 33947605163 scopus 로고    scopus 로고
    • 1117. For examples of pyrrolidine-type catalysts with protic groups
    • (f) Vishnumaya; Singh, V. K. Org. Lett. 2007, 9, 1117. For examples of pyrrolidine-type catalysts with protic groups:
    • (2007) Org. Lett , vol.9
    • Vishnumaya1    Singh, V.K.2
  • 34
    • 33846632873 scopus 로고    scopus 로고
    • Approaches to recyclable organocatalysts for Michael additions, Soluble polymers: (a) Gu, L.; Wu, Y.; Zhang, Y.; Zhao, G. J. Mol. Catal. A 2007, 263, 186. Ionic liquids:
    • Approaches to recyclable organocatalysts for Michael additions, Soluble polymers: (a) Gu, L.; Wu, Y.; Zhang, Y.; Zhao, G. J. Mol. Catal. A 2007, 263, 186. Ionic liquids:
  • 36
    • 4544281440 scopus 로고    scopus 로고
    • Kotrusz, P.; Toma, S.; Schmalz, H.; Adler, A. Eur. J. Org. Chem. 2004, 7, 1577. Fluorous catalysts:
    • (c) Kotrusz, P.; Toma, S.; Schmalz, H.; Adler, A. Eur. J. Org. Chem. 2004, 7, 1577. Fluorous catalysts:
  • 41
    • 34848883078 scopus 로고    scopus 로고
    • The configuration of the chiral center in the cyclohexanone ring of 9a indicates that attack to β-nitrostyrene by the intermediate enamine takes place by the face opposite to the triazolylmethyl substituent
    • The configuration of the chiral center in the cyclohexanone ring of 9a indicates that attack to β-nitrostyrene by the intermediate enamine takes place by the face opposite to the triazolylmethyl substituent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.