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