A facile access to aryl α-sialosides: The combination of a volatile amine base and acetonitrile in glycosidation of sialosyl chlorides

Atsuhito Kuboki, Takahiro Sekiguchi, Takeshi Sugai, Hiromichi Ohta

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

We have succeeded in achieving a facile access to 4-nitrophenyl and 4-methylumbelliferyl-α-sialosides. To sialosyl chlorides which are fully protected with acetyl groups as glycosyl donors, the action of phenols with diisopropylethylamine in acetonitrile brought about high yield as well as facile product isolation.

Original languageEnglish
Pages (from-to)479-482
Number of pages4
JournalSynlett
Issue number5
DOIs
Publication statusPublished - 1998 May

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'A facile access to aryl α-sialosides: The combination of a volatile amine base and acetonitrile in glycosidation of sialosyl chlorides'. Together they form a unique fingerprint.

Cite this