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Volumn 10, Issue 34, 2012, Pages 6987-6994

Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: Application to the synthesis of cascarillic acid, grenadamide and l-(-)-CCG-II

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL EPOXIDES; CYCLOPROPANATION; DIASTEREOSELECTIVE; ENANTIO; NATURAL PRODUCTS; WADSWORTH-EMMONS;

EID: 84864976711     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25622c     Document Type: Article
Times cited : (19)

References (90)
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    • 1H NMR spectroscopy where the methylene hydrogen of ester functionality resonated with a highly diagnostic downfield chemical shift of >4 ppm. According to the literature report, the methylene proton of the cis compound is known to exhibit an upfield shift to 3.74; for a detailed explanation to distinguish cis and trans-cyclopropyl ester, see the ESI of
    • C. D. Bray G. D. Faveri J. Org. Chem. 2010 75 4652
    • (2010) J. Org. Chem. , vol.75 , pp. 4652
    • Bray, C.D.1    Faveri, G.D.2
  • 59
    • 52049117459 scopus 로고    scopus 로고
    • -1 for 3c). The ee of 3a is based on comparison of the optical rotation with the reported value
    • P. Panne A. DeAnglesi J. M. Fox Org. Lett. 2008 10 2987
    • (2008) Org. Lett. , vol.10 , pp. 2987
    • Panne, P.1    Deanglesi, A.2    Fox, J.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.