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Volumn 53, Issue 20, 2014, Pages 5161-5164

Desymmetrization of diolefinic diols by enantioselective amino-thiocarbamate-catalyzed bromoetherification: Synthesis of chiral spirocycles

Author keywords

asymmetric catalysis; chemoselectivity; cyclization; furans; Lewis base

Indexed keywords

CATALYSIS; CATALYSTS; CYCLIZATION;

EID: 84900014384     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201310136     Document Type: Article
Times cited : (83)

References (80)
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    • For selected early efforts, see
    • C. K. Tan, Y.-Y. Yeung, Chem. Commun. 2013, 49, 7985. For selected early efforts, see
    • (2013) Chem. Commun. , vol.49 , pp. 7985
    • Tan, C.K.1    Yeung, Y.-Y.2
  • 72
    • 78650580819 scopus 로고    scopus 로고
    • Triphenylphosphine sulfide was found to be superior in catalyzing the cyclization reactions after screening some catalysts. For details, see TablesS5 and S6. For a related study on using triphenylphosphine sulfide as the catalyst in halocyclization, see:, S. E. Denmark, M. T. Burk, Proc. Natl. Acad. Sci. USA 2010, 107, 20655.
    • (2010) Proc. Natl. Acad. Sci. USA , vol.107 , pp. 20655
    • Denmark, S.E.1    Burk, M.T.2
  • 73
    • 84900005781 scopus 로고    scopus 로고
    • CCDC963942 (7) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC963942 (7) 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.