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Merck
CN

Preparation of 2-iodo allylic alcohols from 2-butyn-1,4-diol.

The Journal of organic chemistry (2008-01-17)
Douglass F Taber, M Inthikhab Sikkander, James F Berry, Kevin J Frankowski
摘要

The conversion of 2-butyn-1,4-diol to (Z)-2,4-diiodobut-2-en-1-ol proceeded efficiently using in situ generated trimethylsilyl iodide. Coupling with Grignard reagents and other nucleophiles delivered (2Z)-2-iodo allylic alcohols. The geometry of the products was established by nOe.

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Sigma-Aldrich
2-丁炔-1,4-二醇, 99%