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Volumn , Issue 24, 2007, Pages 3963-3976

Uronic acids in oligosaccharide synthesis

Author keywords

Carbohydrates; Glycosylation; Oxidation; TEMPO; Uronic acids

Indexed keywords


EID: 34548132442     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700101     Document Type: Short Survey
Times cited : (71)

References (158)
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    • Initially it was established that coupling between two D-galacturonic acid esters could not be effected when using bromide, trichloroacetimidate, and n-pentenyl-functionalized donors.
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    • It had already been found by Dilhas and Bonnaffé that iduronyl imidate donors have superior reactivity to their iduronyl bromide counterparts: A. Dilhas, D. Bonnaffé, Tetrahedron Lett. 2004, 45, 3643-3645.
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    • The authors also tried the little known tris(4-bromophenyl)ammonium hexachloroantimonate without success: A. Marra, J.-M. Mallet, C. Amatore, P. Sinaÿ, Synlett 1990, 572-574.
    • The authors also tried the little known tris(4-bromophenyl)ammonium hexachloroantimonate without success: A. Marra, J.-M. Mallet, C. Amatore, P. Sinaÿ, Synlett 1990, 572-574.
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    • 2O showed no productive coupling between mannuronic acid donors and deactivated acceptor species.
    • 2O showed no productive coupling between mannuronic acid donors and deactivated acceptor species.


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