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Volumn 2014, Issue 16, 2014, Pages 3341-3345

Stereoselective access to β-C-glycosamines by nitro-Michael addition of organolithium reagents

Author keywords

Carbohydrates; Diastereoselectivity; Lithium; Michael addition; Synthetic methods

Indexed keywords


EID: 84901340844     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201402001     Document Type: Article
Times cited : (15)

References (50)
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    • During the preparation of this manuscript, Avenoza and Peregrina reported the addition of an α-selective lithium enolate to nitro galactals, see.
    • During the preparation of this manuscript, Avenoza and Peregrina reported the addition of an α-selective lithium enolate to nitro galactals, see:, C. Aydillo, C. D. Navo, J. H. Busto, F. Corzana, M. M. Zurbano, A. Avenoza, J. M. Peregrina, J. Org. Chem. 2013, 78, 10968-10977.
    • (2013) J. Org. Chem. , vol.78 , pp. 10968-10977
    • Aydillo, C.1    Navo, C.D.2    Busto, J.H.3    Corzana, F.4    Zurbano, M.M.5    Avenoza, A.6    Peregrina, J.M.7
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    • For a similar strategy of Michael addition with organocopper reagents on 2-formylglycals, see.
    • For a similar strategy of Michael addition with organocopper reagents on 2-formylglycals, see:, J. Cossy, H. Rakotoarisoa, Synlett 2000, 734-736.
    • (2000) Synlett , pp. 734-736
    • Cossy, J.1    Rakotoarisoa, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.