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Volumn 52, Issue 35, 2013, Pages 9176-9181

Palladium-catalyzed asymmetric construction of vicinal all-carbon quaternary stereocenters and its application to the synthesis of cyclotryptamine alkaloids

Author keywords

alkaloids; allylic alkylation; asymmetric catalysis; palladium; quaternary stereocenters

Indexed keywords

ALLYLIC ALKYLATION; ASYMMETRIC CATALYSIS; ENANTIOSELECTIVE; FORMAL SYNTHESIS; ITS APPLICATIONS; PALLADIUM-CATALYZED; QUATERNARY STEREOCENTERS;

EID: 84882988062     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201302805     Document Type: Article
Times cited : (138)

References (54)
  • 47
    • 34547844060 scopus 로고    scopus 로고
    • Prior work by Cossy and co-workers has shown that an oxindole dimer can undergo the Pd-catalyzed decarboxylative allylation to construct two vicinal quaternary stereocenters in racemic form. See, C. Menozzi, P. I. Dalko, J. Cossy, Heterocycles 2007, 72, 199.
    • (2007) Heterocycles , vol.72 , pp. 199
    • Menozzi, C.1    Dalko, P.I.2    Cossy, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.