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Volumn 18, Issue 8, 1999, Pages 937-959

Synthesis of carbohydrates with an anomeric thiol moiety for elaboration into metabolically stable thioglycosides

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Indexed keywords


EID: 0033474454     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328309908544045     Document Type: Article
Times cited : (26)

References (50)
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    • (1996) Modern Methods in Carbohydrate Synthesis , pp. 378-402
    • Roy, R.1
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    • Z.J. Witczak, K.A. Nieforth, Eds.; MDI: New York
    • R. Roy, in Carbohydrates in Drug Design, Z.J. Witczak, K.A. Nieforth, Eds.; MDI: New York, 1997, pp 83-135.
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    • P. Kovác in Modern Methods in Carbohydrate Synthesis, S.H. Khan, R.A. O'Neill, Eds.; Harwood Academic: Amsterdam, 1996, pp 55-81.
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    • The formation of a Gal disulfide derivative during NaOMe catalysed anomeric thioacetate deprotection has recently been mentioned in: U.J. Nilsson, E.J.-L. Fournier and O. Hindsgaul, Bioorg. Med. Chem., 6, 1563 (1998).
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 1563
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    • formula presented
    • Disulfide 41 was prepared by TMSOTf mediated coupling between the sialosyl phosphite i and the disulfide 21 using the method described by T.J. Martin and R.R. Schmidt, Tetrahedron Lett., 33, 6123 (1992). (formula presented)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.