Mono-Triflation of carbohydrate diols and triols

Spencer Knapp, Andrew B.J. Naughton, Paivi J. Kukkola, Wen Chung Shieh

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

For five carbohydrate substrates [methyl 4, 6-0-(phenylmethylene)-l-thio-a-D-glucopyranoside la, l-cyano-l-deoxy-4, 6-0-(phenylmethylene)-a-D-galactopyranose 2a, methyl a-D-xylopyranoside 3a, methyl p-D-arabinopyranoside 4a, and methyl 5-0-(ferr-butyldiphenylsUyl)-a-D-ribofuranoside 5a], selective mono-triflation was achieved where the reacting hydroxyl is cis and vicinal to a heteroatom.

Original languageEnglish (US)
Pages (from-to)981-993
Number of pages13
JournalJournal of Carbohydrate Chemistry
Volume10
Issue number6
DOIs
StatePublished - Jan 1 1991

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Mono-Triflation of carbohydrate diols and triols'. Together they form a unique fingerprint.

Cite this