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Volumn 19, Issue 23, 2013, Pages 7319-7323

Organocatalytic Michael addition of malonates to isatylidene-3- acetaldehydes: Application to the total synthesis of (-)-debromoflustramine e

Author keywords

asymmetric synthesis; enantioselectivity; Michael addition; organocatalysis; oxindoles

Indexed keywords

ASYMMETRIC SYNTHESIS; ASYMMETRIC TOTAL SYNTHESIS; CONJUGATE ADDITION; ENANTIOSELECTIVE SYNTHESIS; MICHAEL ADDITIONS; ORGANOCATALYSIS; OXINDOLES; SYNTHETIC UTILITY;

EID: 84878245658     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201300977     Document Type: Article
Times cited : (39)

References (111)
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    • 79952165881 scopus 로고    scopus 로고
    • For two ester groups, Shi and co-workers have reported a Lewis base catalyzed, highly regioselective cycloaddition reaction first initiated at the β-position:, X.-C. Zhang, S.-H. Cao, Y. Wei, M. Shi, Org. Lett. 2011, 13, 1142.
    • (2011) Org. Lett. , vol.13 , pp. 1142
    • Zhang, X.-C.1    Cao, S.-H.2    Wei, Y.3    Shi, M.4
  • 88
    • 84858684821 scopus 로고    scopus 로고
    • Kwiatkowski recently reported the construction of β-carbonyl- substituted quaternary stereogenic centers from α,β-unsaturated enones at high pressure with low to moderate ee:, D. Łyżwa, K. Dudziński, P. Kwiatkowski, Org. Lett. 2012, 14, 1540.
    • (2012) Org. Lett. , vol.14 , pp. 1540
    • Łyzwa, D.1    Dudziński, K.2    Kwiatkowski, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.