메뉴 건너뛰기




Volumn 48, Issue 31, 2009, Pages 5737-5740

Chemoselective asymmetric n-allylic alkylation of indoles with morita-baylis-hillman carbonates

Author keywords

Chemoselectivity; Indoles; Morita Baylis Hillman carbonates; N allylic alkylation; Organocatalysis

Indexed keywords

CHEMOSELECTIVITY; INDOLES; MORITA-BAYLIS-HILLMAN CARBONATES; N-ALLYLIC ALKYLATION; ORGANOCATALYSIS;

EID: 70349783582     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902093     Document Type: Article
Times cited : (239)

References (48)
  • 4
    • 22944454156 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: a) S. Cacchi, G. Fabrizi, Chem. Rev. 2005, 105, 2873;
    • (2005) Chem. Rev , vol.105 , pp. 2873
    • Cacchi, S.1    Fabrizi, G.2
  • 34
    • 48849104472 scopus 로고    scopus 로고
    • For metal-catalyzed C3-selective allylic alkylation of indoles, see: a W.-B. Liu, H. He, L.-X. Dai, S.-L. You, Org. Lett. 2008, 10, 1815;
    • For metal-catalyzed C3-selective allylic alkylation of indoles, see: a) W.-B. Liu, H. He, L.-X. Dai, S.-L. You, Org. Lett. 2008, 10, 1815;
  • 38
    • 4544324311 scopus 로고    scopus 로고
    • either C3- or N-selective allylic alkylation products could be obtained in a racemic form, see: e M. Bandini, A. Melloni, A. Umani-Ronchi, Org. Lett. 2004, 6, 3199.
    • either C3- or N-selective allylic alkylation products could be obtained in a racemic form, see: e) M. Bandini, A. Melloni, A. Umani-Ronchi, Org. Lett. 2004, 6, 3199.
  • 39
    • 66149122216 scopus 로고    scopus 로고
    • For a base-catalyzed C3-selective alkylation of indoles, see: M. Bandini, R. Sinisi, Org. Lett. 2009, 11, 2093.
    • For a base-catalyzed C3-selective alkylation of indoles, see: M. Bandini, R. Sinisi, Org. Lett. 2009, 11, 2093.
  • 40
    • 70349932365 scopus 로고    scopus 로고
    • 3.
    • 3.
  • 42
    • 70349921022 scopus 로고    scopus 로고
    • For more screening studies, see the Supporting Information
    • For more screening studies, see the Supporting Information.
  • 43
    • 70349895295 scopus 로고    scopus 로고
    • CCDC 732289 (3 o) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
    • CCDC 732289 (3 o) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 46
    • 70349906504 scopus 로고    scopus 로고
    • see the Supporting Information
    • b) see the Supporting Information.
  • 47
    • 54049137275 scopus 로고    scopus 로고
    • For the synthesis of the core structure of Yuremamine in five steps, see: a M. B. Johansen, M. A. Kerr, Org. Lett. 2008, 10, 3497;
    • For the synthesis of the core structure of Yuremamine in five steps, see: a) M. B. Johansen, M. A. Kerr, Org. Lett. 2008, 10, 3497;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.