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Volumn 7, Issue 15, 2009, Pages 3095-3101

Enantioselective synthesis of highly functionalized octahydro-6-oxo-1- phenylnaphthalene-2-carbaldehydes via organocatalytic domino reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL CONDENSATION; CARBALDEHYDES; CINNAMALDEHYDE; DIASTEREO-SELECTIVITY; DOMINO REACTIONS; ENANTIOSELECTIVE SYNTHESIS; FUNCTIONALIZED; HIGH ENANTIOSELECTIVITY; MICHAEL REACTIONS; ORGANOCATALYTIC; PHENYLNAPHTHALENE; X-RAY ANALYSIS;

EID: 68949146804     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b906205j     Document Type: Article
Times cited : (31)

References (80)
  • 73
    • 0000116562 scopus 로고    scopus 로고
    • In some organocatalytic reactions, the use of a more acidic co-catalyst could deprotect the silyl ether on the catalyst with concomitant deactivation of the catalyst, resulting in a slower reaction rate and low yields. For examples, see:
    • J. B. Schwarz A. I. Meyers J. Org. Chem. 1998 63 1732
    • (1998) J. Org. Chem. , vol.63 , pp. 1732
    • Schwarz, J.B.1    Meyers, A.I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.