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Volumn 353, Issue 14-15, 2011, Pages 2671-2675

Highly enantioselective conjugate addition-cyclization cascade reaction of malonates with o-hydroxycinnamaldehydes: Asymmetric synthesis of 4-substituted chromanols

Author keywords

asymmetric synthesis; chromans; conjugate addition; malonates; organocatalysts

Indexed keywords


EID: 80054737705     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100324     Document Type: Article
Times cited : (46)

References (55)
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    • For organocatalytic conjugate addition of malonates to α,β-unsaturated aldehydes, see: I. Fleischer, A. Pfaltz, Chem. Eur. J. 2010, 16, 95
    • (2010) Chem. Eur. J. , vol.16 , pp. 95
    • Fleischer, I.1    Pfaltz, A.2
  • 42
    • 53849098072 scopus 로고    scopus 로고
    • For recent examples having the similar strategy on organocatalytic conjugate addition-cyclization cascade reaction, see: M. Rueping, E. Merino, E. Sugiono, Adv. Synth. Catal. 2008, 350, 2127
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2127
    • Rueping, M.1    Merino, E.2    Sugiono, E.3
  • 45
    • 77950795873 scopus 로고    scopus 로고
    • For examples of the phenol OH group which has served as nucleophile, see: M. Rueping, M.-Y. Lin, Chem. Eur. J. 2010, 16, 4169
    • (2010) Chem. Eur. J. , vol.16 , pp. 4169
    • Rueping, M.1    Lin, M.-Y.2
  • 53
    • 33745715054 scopus 로고    scopus 로고
    • For a review on MacMillan′s imidazolidinone catalyst, see.
    • For a review on MacMillan′s imidazolidinone catalyst, see:, G. Lelais, D. W. C. MacMillan, Aldrichimica Acta 2006, 39, 79.
    • (2006) Aldrichimica Acta , vol.39 , pp. 79
    • Lelais, G.1    MacMillan, D.W.C.2
  • 54
    • 51749084445 scopus 로고    scopus 로고
    • For a review of diarylprolinol silyl ether as catalyst, see.
    • For a review of diarylprolinol silyl ether as catalyst, see:, A. Mielgo, C. Palomo, Chem. Asian J. 2008, 3, 922.
    • (2008) Chem. Asian J. , vol.3 , pp. 922
    • Mielgo, A.1    Palomo, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.