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Volumn 47, Issue 18, 2008, Pages 3414-3417

Organocatalytic asymmetric formal [3+2] cycloaddition reaction of isocyanoesters to nitroolefins leading to highly optically active dihydropyrroles

Author keywords

Asymmetric catalysis; Cinchona alkaloids; Enantioselectivity; Isocyanoesters; Pyrroles

Indexed keywords

CHEMICAL REACTIONS; ENANTIOSELECTIVITY;

EID: 43849090515     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800003     Document Type: Article
Times cited : (170)

References (54)
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    • Houk, K.N.1    List, B.2
  • 15
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    • Seminal work on the enantioselective aldol reaction between isocyanoesters and carbonyl compounds: a Y. Ito, M. Samura, T. Hayashi, J. Am. Chem. Soc. 1986, 108, 6405.
    • Seminal work on the enantioselective aldol reaction between isocyanoesters and carbonyl compounds: a) Y. Ito, M. Samura, T. Hayashi, J. Am. Chem. Soc. 1986, 108, 6405.
  • 16
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    • For a review, see: b, Ed, I. Ojima, Wiley-VCH, Weinheim
    • For a review, see: b) M. Sawamura, Y. Ito, In Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 1993, pp. 367.
    • (1993) In Catalytic Asymmetric Synthesis , pp. 367
    • Sawamura, M.1    Ito, Y.2
  • 50
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    • The reaction of methylisocyano acetate with 2k gave a complex product mixture that did not contain the desired compound.
    • The reaction of methylisocyano acetate with 2k gave a complex product mixture that did not contain the desired compound.
  • 54
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    • Eds, J. Zhu, H. Bienayme, Wiley-VCH, Weinheim
    • Multicomponent Reactions (Eds.: J. Zhu, H. Bienayme), Wiley-VCH, Weinheim, 2005.
    • (2005) Multicomponent Reactions


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.