By the same authors

From the same journal

A one-step procedure for the monoacylation of symmetrical 1,2-diols

Research output: Contribution to journalArticle

Author(s)

  • P A Clarke
  • N E Kayaleh
  • M A Smith
  • J R Baker
  • S J Bird
  • C Chan

Department/unit(s)

Publication details

JournalJournal of Organic Chemistry
DatePublished - 26 Jul 2002
Issue number15
Volume67
Number of pages6
Pages (from-to)5226-5231
Original languageEnglish

Abstract

A series of lanthanide (III) salts have been shown to catalyze the monoacylation of symmetrical 1,2-diols by carboxylic acid anhydrides with surprisingly high selectivity.

    Research areas

  • EFFICIENT ESTERIFICATION REACTION, SELECTIVE MONOACYLATION, LEWIS-ACID, SCANDIUM TRIFLUOROMETHANESULFONATE, 10-DEACETYL BACCATIN, ORGANIC-REACTIONS, MIXED ANHYDRIDES, ALUMINA SURFACES, CATALYTIC AMOUNT, RING-CLEAVAGE

Research outputs

Discover related content

Find related publications, people, projects, datasets and more using interactive charts.

View graph of relations