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Volumn 356, Issue 11-12, 2014, Pages 2697-2702

6-azabicyclo[3.2.1]octanes via copper-catalyzed enantioselective alkene carboamination

Author keywords

6 azabicyclo 3.2.1 octanes; alkaloids; carboamination; copper catalyzed reactions; enantioselectivity

Indexed keywords


EID: 84906278475     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400317     Document Type: Article
Times cited : (20)

References (37)
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    • 79851489841 scopus 로고    scopus 로고
    • Q. Li, X. Jiang, C. Fu, S. Ma, Org. Lett. 2011, 13, 466. For related synthesis of [3.3.1]azabicycles using asymmetric catalysis, see
    • (2011) Org. Lett. , vol.13 , pp. 466
    • Li, Q.1    Jiang, X.2    Fu, C.3    Ma, S.4
  • 34
    • 84886423064 scopus 로고    scopus 로고
    • The pro-S and pro-R transition states for similar reactions have been modeled with density functional theory calculations:, L. Belding, S. R. Chemler, T. Dudding, J. Org. Chem. 2013, 78, 10288.
    • (2013) J. Org. Chem. , vol.78 , pp. 10288
    • Belding, L.1    Chemler, S.R.2    Dudding, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.