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Volumn , Issue 26, 2012, Pages 4927-4930

Halide effects on cyclopropenium cation promoted glycosylation with deoxy sugars: Highly α-selective glycosylations using a 3,3-dibromo-1,2- diphenylcyclopropene promoter

Author keywords

Carbohydrates; Diastereoselectivity; Glycosylation; Synthetic methods

Indexed keywords


EID: 84865740723     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201200907     Document Type: Article
Times cited : (42)

References (96)
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  • 15
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    • The 4,6-benzylidene acetal does not provide stereoselective glycosylations in the 2-deoxy sugar series, see:, D. Crich, O. Vinogradova, J. Org. Chem. 2006, 71, 8473-8480.
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    • Shan, M.1    Sharif, E.U.2    O'Doherty, G.A.3
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    • (2011) Angew. Chem. , vol.123 , pp. 12430-12434
    • Vanos, C.M.1    Lambert, T.H.2
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    • Wulff, G.1    Röhle, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.