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Volumn 52, Issue 43, 2013, Pages 11269-11272

Enantioselective total synthesis of (-)-minovincine in nine chemical steps: An approach to ketone activation in cascade catalysis

Author keywords

alkaloids; enantioselectivity; natural products; organocatalysis; total synthesis

Indexed keywords

DIELS-ALDER; ENANTIOSELECTIVE TOTAL SYNTHESIS; LEAVING GROUPS; NATURAL PRODUCTS; ORGANOCATALYSIS; TOTAL SYNTHESIS;

EID: 84885576894     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201305171     Document Type: Article
Times cited : (73)

References (28)
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  • 13
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    • For a semisynthesis of (-)-minovincine beginning from vindoline, see:, N. Langlois, R. Z. Andriamialiosa, J. Org. Chem. 1979, 44, 2468-2471.
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    • Langlois, N.1    Andriamialiosa, R.Z.2
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  • 28
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    • For an example of L -Selectride 1,4-conjugate reduction of a vinylogous amide, see:, T. J. Donohoe, M. J. Connolly, L. Walton, Org. Lett. 2009, 11, 5562-5565.
    • (2009) Org. Lett. , vol.11 , pp. 5562-5565
    • Donohoe, T.J.1    Connolly, M.J.2    Walton, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.