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Volumn 11, Issue 9, 2009, Pages 1927-1930

Rational design of organocatalyst: Highly stereoselective michael addition of cyclic ketones to nitroolefins

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[No Author keywords available]

Indexed keywords


EID: 66149154333     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900330p     Document Type: Article
Times cited : (113)

References (48)
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    • Berkessel, A, Gröger, H, Eds, Wiley-VCH: Weinheim
    • (f) Asymmetric Organocatalysis; Berkessel, A., Gröger, H., Eds.; Wiley-VCH: Weinheim, 2005.
    • (2005) Asymmetric Organocatalysis
  • 7
    • 55049138759 scopus 로고    scopus 로고
    • Dalko, P. I, Ed.;Wiley-VCH: Weinheim
    • (g) Enantioselective Organocatalysis; Dalko, P. I., Ed.;Wiley-VCH: Weinheim, 2007.
    • (2007) Enantioselective Organocatalysis
  • 18
    • 0034812506 scopus 로고    scopus 로고
    • Enamine-based Michael reaction of carbonyl compounds with nitroolefins: (a) Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F., III. J.Am. Chem. Soc. 2001, 123, 5260.
    • Enamine-based Michael reaction of carbonyl compounds with nitroolefins: (a) Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F., III. J.Am. Chem. Soc. 2001, 123, 5260.
  • 24
    • 33645454505 scopus 로고    scopus 로고
    • For selected recent proline derivatives containing H-bond to control stereochemistry, see: a
    • For selected recent proline derivatives containing H-bond to control stereochemistry, see: (a) Knudsen, R. K.; Mitchell, C. E. T.; Ley, S. V. Chem. Commun. 2006, 66.
    • (2006) Chem. Commun , pp. 66
    • Knudsen, R.K.1    Mitchell, C.E.T.2    Ley, S.V.3
  • 29
    • 22144459070 scopus 로고    scopus 로고
    • Control stereochemistry by containing the bulky group: (a) Hayashi, Y.; Gotoh, H.; Hayashi, T.; Shoji, M. Angew. Chem., Int. Ed. 2005, 44, 4212.
    • Control stereochemistry by containing the bulky group: (a) Hayashi, Y.; Gotoh, H.; Hayashi, T.; Shoji, M. Angew. Chem., Int. Ed. 2005, 44, 4212.
  • 33
    • 33646142092 scopus 로고    scopus 로고
    • Containing salt to control stereochemistry: (a) Mase, N.; Watanabe, K.; Yoda, H.; Takabe, K.; Tanaka, F.; Barbas, C. F., III. J. Am. Chem. Soc. 2006, 128, 4966.
    • Containing salt to control stereochemistry: (a) Mase, N.; Watanabe, K.; Yoda, H.; Takabe, K.; Tanaka, F.; Barbas, C. F., III. J. Am. Chem. Soc. 2006, 128, 4966.
  • 36
    • 15744383666 scopus 로고    scopus 로고
    • For some new catalysts containing phosphine, see: a
    • For some new catalysts containing phosphine, see: (a) Shi, M.; Chen, L.; Li, C. J. Am. Chem. Soc. 2005, 127, 3790.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 3790
    • Shi, M.1    Chen, L.2    Li, C.3
  • 39
    • 0000220483 scopus 로고    scopus 로고
    • Reaction of cyclohexanone with nitroolefins: (a) Alexakis, A.; Andrey, O. Org. Lett. 2002, 4, 3611.
    • Reaction of cyclohexanone with nitroolefins: (a) Alexakis, A.; Andrey, O. Org. Lett. 2002, 4, 3611.
  • 46
    • 66149105091 scopus 로고    scopus 로고
    • The application of Michael adduct, see: Ono, N. The Nitro Group in Organic Synthesis; Wiley-VCH: Weiheim, 2001. For selected examples, see: Seamus, H.; Connon, M. C.; Connon, S. J. Org. Lett. 2007, 9, 509.
    • The application of Michael adduct, see: Ono, N. The Nitro Group in Organic Synthesis; Wiley-VCH: Weiheim, 2001. For selected examples, see: Seamus, H.; Connon, M. C.; Connon, S. J. Org. Lett. 2007, 9, 509.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.