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Volumn 8, Issue 19, 2006, Pages 4195-4198

Asymmetric Morita-Baylis-Hillman reaction catalyzed by isophoronediamine- derived bis(thio)urea organocatalysts

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Indexed keywords


EID: 33748989516     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol061298m     Document Type: Article
Times cited : (127)

References (32)
  • 4
    • 0000892247 scopus 로고    scopus 로고
    • Paquette, L. A., Ed; Wiley: New York
    • (d) Ciganek, E. In Organic Reactions; Paquette, L. A., Ed; Wiley: New York, 1997; Vol. 51, p 201.
    • (1997) Organic Reactions , vol.51 , pp. 201
    • Ciganek, E.1
  • 9
    • 27544480807 scopus 로고    scopus 로고
    • For recent advances in the asymmetric aza-Morita-Baylis-Hillman reaction see: (a) Raheem, I. T.; Jacobsen, E. N. Adv. Synth. Catal. 2005, 347, 1701.
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1701
    • Raheem, I.T.1    Jacobsen, E.N.2
  • 23
    • 33749009946 scopus 로고    scopus 로고
    • note
    • X-ray crystallographic data for 1a and 1c are included in the Supporting Information.
  • 25
    • 29844448114 scopus 로고    scopus 로고
    • For recent reviews on catalysis by hydrogen-bond donors see: (a) Takemoto, Y. Org. Biomol. Chem. 2005, 3, 4299.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4299
    • Takemoto, Y.1
  • 31
    • 30144438570 scopus 로고    scopus 로고
    • Polar solvents are assumed to catalyze the MBH reaction by a proton transfer mechanism. The same mechanism presumably underlies the frequently observed autocatalysis by the product, (a) Aggarwal, V. K.; Fulford, S. Y.; Lloyd-Jones, G. C. Angew. Chem., Int. Ed. 2005, 44, 1734.
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1734
    • Aggarwal, V.K.1    Fulford, S.Y.2    Lloyd-Jones, G.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.