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Volumn 75, Issue 5, 2010, Pages 1402-1409

Chiral bifunctional thiourea-catalyzed enantioselective michael addition of ketones to nitrodienes

Author keywords

[No Author keywords available]

Indexed keywords

BIFUNCTIONAL; CHEMICAL EQUATIONS; CHIRAL DIAMINE; ENANTIOSELECTIVE MICHAEL ADDITION; ENANTIOSELECTIVITES; GOOD YIELD; MICHAEL ADDUCTS;

EID: 77949292644     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo901991v     Document Type: Article
Times cited : (101)

References (79)
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    • For reviews of asymmetric Michael addition reactions, see: a, Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: New York, Chapters 31.1 and 31.2, pp
    • For reviews of asymmetric Michael addition reactions, see: (a) Tomioka, K.; Nagaoka, Y.; Yamaguchi, M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York, 1999; Vol. III, Chapters 31.1 and 31.2, pp 1105-1139.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 1105-1139
    • Tomioka, K.1    Nagaoka, Y.2    Yamaguchi, M.3
  • 8
    • 0035886887 scopus 로고    scopus 로고
    • For selected reviews of organocatalysis, see: a
    • For selected reviews of organocatalysis, see: (a) Dalko, P. I.; Moisan, L. Angew. Chem., Int. Ed. 2001, 40, 3726.
    • (2001) Angew. Chem., Int. Ed , vol.40 , pp. 3726
    • Dalko, P.I.1    Moisan, L.2
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    • 34250613134 scopus 로고    scopus 로고
    • For reviews of organocatalytic Michael addition reaction, see: a
    • For reviews of organocatalytic Michael addition reaction, see: (a) Tsogoeva, S. B. Eur. J. Org. Chem. 2007, 1701.
    • (2007) Eur. J. Org. Chem , pp. 1701
    • Tsogoeva, S.B.1
  • 16
    • 29844448114 scopus 로고    scopus 로고
    • For reviews on chiral thiourea promoted organocatalytic reactions: a
    • For reviews on chiral thiourea promoted organocatalytic reactions: (a) Takemoto, Y. Org. Biomol. Chem. 2005, 3, 4299.
    • (2005) Org. Biomol. Chem , vol.3 , pp. 4299
    • Takemoto, Y.1
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    • 33744928626 scopus 로고    scopus 로고
    • Results of organocatalytic Michael addition reactions reported by Jacobsen's group, see: a
    • Results of organocatalytic Michael addition reactions reported by Jacobsen's group, see: (a) Huang, H.; Jacobsen, E. N. J. Am. Chem. Soc. 2006, 128, 7170.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 7170
    • Huang, H.1    Jacobsen, E.N.2
  • 24
    • 0142072631 scopus 로고    scopus 로고
    • Results of organocatalytic Michael addition reactions reported by Takemoto's group, see: a
    • Results of organocatalytic Michael addition reactions reported by Takemoto's group, see: (a) Okino, T.; Hoashi, Y.; Takemoto, Y. J. Am. Chem. Soc. 2003, 125, 12672.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12672
    • Okino, T.1    Hoashi, Y.2    Takemoto, Y.3
  • 30
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    • For the results of organocatalytic Michael addition reactions reported by the Tsogoeva's group, see: a
    • For the results of organocatalytic Michael addition reactions reported by the Tsogoeva's group, see: (a) Tsogoeva, S. B.; Yalalov, D. A.; Hateley, M. J.; Weckbecker, C.; Huthmacher, K. Eur. J. Org. Chem. 2005, 4995.
    • (2005) Eur. J. Org. Chem , pp. 4995
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  • 36
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    • Other chiral thiourea-catalyzed Michael addition reactions; selected examples: (a) McCooey, S. H.; Connon, S. J. Angew. Chem., Int. Ed. 2005, 44, 6367.
    • Other chiral thiourea-catalyzed Michael addition reactions; selected examples: (a) McCooey, S. H.; Connon, S. J. Angew. Chem., Int. Ed. 2005, 44, 6367.
  • 56
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    • Recently, Alexakis and co-workers provided an excellent example of the diphenylprolinol-catalyzed additions of aldehydes to nitrodienes: Belot, S.; Massaro, A.; Tenti, A.; Mordini, A.; Alexakis, A. Org. Lett. 2008, 10, 4557.
    • Recently, Alexakis and co-workers provided an excellent example of the diphenylprolinol-catalyzed additions of aldehydes to nitrodienes: Belot, S.; Massaro, A.; Tenti, A.; Mordini, A.; Alexakis, A. Org. Lett. 2008, 10, 4557.
  • 59
    • 0000220483 scopus 로고    scopus 로고
    • Weak Brønsted acids as additives in asymmetric organocatalytic Michael Addition; see a recent review (ref 4a, Selected recent examples: (a) Alexakis, A, Andrey, O. Org. Lett, 2002, 4, 3611
    • 4a). Selected recent examples: (a) Alexakis, A.; Andrey, O. Org. Lett, 2002, 4, 3611.
  • 69
    • 77949304834 scopus 로고    scopus 로고
    • CCDC 733670 contains the supplementary crystallographic data for the product 3ad, also be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • CCDC 733670 contains the supplementary crystallographic data for the product 3ad. These data can also be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
    • These data can
  • 70
    • 77949304834 scopus 로고    scopus 로고
    • CCDC 698374 and CCDC 695685 contain the supplementary crystallography data for the products 1a and 1g, also be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • CCDC 698374 and CCDC 695685 contain the supplementary crystallography data for the products 1a and 1g. These data can also be obtained free of charge from the Cambridge Crystallographic Data Centre via www. ccdc.cam.ac.uk/data- request/cif.
    • These data can


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.