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Volumn 11, Issue 21, 2005, Pages 6159-6174

Combinatorial synthesis of an oligosaccharide library by using β-bromoglycoside-mediated iterative glycosylation of selenoglycosides: Rapid expansion of molecular diversity with simple building blocks

Author keywords

Carbohydrates; Chalcogens; Combinatorial chemistry; Glycosylation; Oligosaccharides

Indexed keywords

CHALCOGENS; COMBINATORIAL CHEMISTRY; GLYCOSYLATION; OLIGOSACCHARIDES;

EID: 27344443883     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200500126     Document Type: Article
Times cited : (39)

References (121)
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    • b) glycosylation of the β-bormoglycoside donor with selenoglycoside acceptor by the action of silver salt has been reported; see, S. Mehta, B. M. Pinto, J. Org. Chem. 1993, 58, 3269. However, the glycosylation was not observed under the conditions reported in this manuscript.
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    • While two stereoisomers with respect to the orthoester quaternary carbon center might form in 4, namely exo- and endo-isomer, only the exo-isomer was formed as judged by the existence of the nuclear overhauser effect from the methoxy proton to C1- and C2-protons in the NOESY experiments. R. U. Lemieux, A. R. Morgan, Can. J. Chem. 1965, 43, 2199.
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    • and references therein
    • For details of our interests in organotellurium compounds in synthesis, see S. Yamago, Synlett 2004, 1875, and references therein.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.