UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

3,5-Isoxazoles from alpha-bromo-pentafluorophenyl vinylsulfonates: Synthesis of sulfonates and sulfonamides

Lee, CC; Fitzmaurice, RJ; Caddick, S; (2009) 3,5-Isoxazoles from alpha-bromo-pentafluorophenyl vinylsulfonates: Synthesis of sulfonates and sulfonamides. ORG BIOMOL CHEM , 7 (21) 4349 - 4351. 10.1039/b911098d.

Full text not available from this repository.

Abstract

The regioselective 1,3-dipolar cycloaddition of alpha-bromo-pentafluorophenyl vinylsulfonate with nitrile oxides has been used to rapidly access a range of 3,5-isoxazoles which could be converted directly to their corresponding sulfonamides.

Type:Article
Title:3,5-Isoxazoles from alpha-bromo-pentafluorophenyl vinylsulfonates: Synthesis of sulfonates and sulfonamides
DOI:10.1039/b911098d
Keywords:1,3-DIPOLAR CYCLOADDITION, NITRILE OXIDES, ISOXAZOLES, ANALOGS, DERIVATIVES, NUCLEOSIDE, INHIBITORS
UCL classification:UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry
UCL > VP Enterprise

Archive Staff Only: edit this record