Autor:	Paivi J. Kukkola, Spencer Knapp, Andrew B. J. Naughton, Wen Chung Shieh
Rok vydání:	1991
Předmět:	Chemistry Stereochemistry Organic Chemistry Heteroatom Organic chemistry Carbohydrate Biochemistry Vicinal
Zdroj:	Journal of Carbohydrate Chemistry. 10:981-993
ISSN:	1532-2327 0732-8303
DOI:	10.1080/07328309108543967
Popis:	For five carbohydrate substrates [methyl 4,6-O-(phenylmethylene)-1-thio-α-D-glucopyranoside 1a, 1-cyano-1-deoxy-4,6-O-(phenylmethylene)-α-D-galactopyranose 2a, methyl α-D-xylopyranoside 3a, methyl β-D-arabinopyranoside 4a, and methyl 5-O-(tert-butyldiphenylsilyl)-α-D-ribofuranoside 5a], selective mono-triflation was achieved where the reacting hydroxyl is cis and vicinal to a heteroatom.
Databáze:	OpenAIRE
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