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Volumn 60, Issue 35, 2004, Pages 7705-7714

Enantioselective organocatalytic aldehyde-aldehyde cross-aldol couplings. The broad utility of α-thioacetal aldehydes

Author keywords

Aldol; Catalysis; Diastereoselection; Enantioselective; Organocatalysis; Proline

Indexed keywords

KETONE; PROLINE; THIOACETALDEHYDE;

EID: 3843118994     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.089     Document Type: Article
Times cited : (96)

References (60)
  • 1
    • 0036105811 scopus 로고    scopus 로고
    • For some reviews of the aldol reaciton see: (a)
    • For some reviews of the aldol reaciton see: (a) Alcaide B., Almendros P. Eur. J. Org. Chem. 2002;1595
    • (2002) Eur. J. Org. Chem. , pp. 1595
    • Alcaide, B.1    Almendros, P.2
  • 13
    • 0000584420 scopus 로고
    • Morrion J.D. New York: Academic
    • Heathcock C.H. Morrion J.D. Asymmetric Synthesis. Vol. 3:1984;111 Academic, New York
    • (1984) Asymmetric Synthesis , vol.3 , pp. 111
    • Heathcock, C.H.1
  • 21
    • 0000145196 scopus 로고
    • The Directed Aldol Reaction
    • New York: Wiley. p 203
    • Mukaiyama T. The Directed Aldol Reaction. Organic Reactions. Vol. 28:1982;Wiley, New York. p 203
    • (1982) Organic Reactions , vol.28
    • Mukaiyama, T.1
  • 52
    • 3843122741 scopus 로고    scopus 로고
    • Crystallographic data have been deposited at the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK and copies can be obtained on request, free of charge, by quoting the publication citation and the deposition number 235290
    • Crystallographic data have been deposited at the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK and copies can be obtained on request, free of charge, by quoting the publication citation and the deposition number 235290


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.