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Stereochemical control of the glycosylation reaction via 3,5-di-O-(p-toluoyl)-2-O-(p-toluolsulfonyl)-β-D-methyl ribofuranoside

✍ Scribed by Christos Papageorgiou; Christoph Tamm

Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 195 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)84038-1

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✦ Synopsis

Lewis acid catalyzed glycosylation of the 2'-tosyl ribofuranose derivative jj leads exclusively to fi-nucleosides in the uridine and adenosine series.

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