UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Selective Conversion of Alcohols into Alkyl Iodides Using a Thioiminium Salt

Ellwood, AR; Porter, MJ; (2009) Selective Conversion of Alcohols into Alkyl Iodides Using a Thioiminium Salt. J ORG CHEM , 74 (20) 7982 - 7985. 10.1021/jo901415n.

Full text not available from this repository.

Abstract

Treatment of a range of primary and secondary alcohols with MeSCH=NMe2+ I- affords the corresponding alkyl iodides in excellent yield with straightforward purification. Selective formation of a primary iodide in the presence of a secondary alcohol can be achieved.

Type:Article
Title:Selective Conversion of Alcohols into Alkyl Iodides Using a Thioiminium Salt
DOI:10.1021/jo901415n
Keywords:CHLOROTRIMETHYLSILANE SODIUM IODIDE, HYDROXYL-GROUPS, REAGENT SYSTEM, EFFICIENT, HALIDES, REPLACEMENT, HALOGENATION, CONVENIENT, INVERSION, SULFIDES
UCL classification:UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry

Archive Staff Only: edit this record