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Volumn 10, Issue 16, 2008, Pages 3489-3492

A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CYCLOPENTANE DERIVATIVE; ETHYLENE OXIDE; TOLUENE;

EID: 54049089022     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801273x     Document Type: Article
Times cited : (99)

References (58)
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    • (1993) Chem. Rev , vol.93 , pp. 2037
    • Fuji, K.1
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    • Reviews of synthesis and bioactivities of cyclopentanes: a
    • Reviews of synthesis and bioactivities of cyclopentanes: (a) Silva, L. F. Tetrahedron 2002, 58, 9137.
    • (2002) Tetrahedron , vol.58 , pp. 9137
    • Silva, L.F.1
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    • 33746277515 scopus 로고    scopus 로고
    • For books and selected recent reviews on organocatalysis, see: a
    • For books and selected recent reviews on organocatalysis, see: (a) Connon, S. J. Chem. Eur. J. 2006, 12, 5418.
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    • Connon, S.J.1
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    • 0037020389 scopus 로고    scopus 로고
    • For selected reviews regarding Michel addition reactions, see: a
    • For selected reviews regarding Michel addition reactions, see: (a) Koichi, M.; Terada, M.; Hiroshi, M. Angew. Chem., Int. Ed. 2002, 41, 3554.
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 3554
    • Koichi, M.1    Terada, M.2    Hiroshi, M.3
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    • 4143136647 scopus 로고    scopus 로고
    • For developments and applications of cinchona-derived bifunctional catalysts, see: a
    • For developments and applications of cinchona-derived bifunctional catalysts, see: (a) Tian, S.-K.; Chen, Y.; Hang, J.; Tang, L.; McDaid, P.; Deng, L. Acc. Chem. Res. 2004, 37, 621.
    • (2004) Acc. Chem. Res , vol.37 , pp. 621
    • Tian, S.-K.1    Chen, Y.2    Hang, J.3    Tang, L.4    McDaid, P.5    Deng, L.6
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    • Tan, B.; Chua, P. J.; Li, Y.; Zhong, G. Org. Lett. 2008, 10, 2437. The results of forming chiral cyclohexanes with excellent enantioselectivities (97 to >99% ee) and high diastereoselectivities (93:7-99:1 dr) were reported.
    • Tan, B.; Chua, P. J.; Li, Y.; Zhong, G. Org. Lett. 2008, 10, 2437. The results of forming chiral cyclohexanes with excellent enantioselectivities (97 to >99% ee) and high diastereoselectivities (93:7-99:1 dr) were reported.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.