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原硅酸酯介导的单取代次膦酸的酯化反应。

Orthosilicate-mediated esterification of monosubstituted phosphinic acids.

作者信息

Dumond YR, Baker RL, Montchamp JL

机构信息

Department of Chemistry, Box 298860, Texas Christian University, Fort Worth, Texas 76129, USA.

出版信息

Org Lett. 2000 Oct 19;2(21):3341-4. doi: 10.1021/ol006434g.

DOI:10.1021/ol006434g
PMID:11029205
Abstract

Monosubstituted phosphinic acids are esterified with orthosilicates in excellent yields. Phosphinylidene-containing acids react selectively under these conditions, while disubstituted phosphinic acids and phosphonic acids remain unchanged. One-pot procedures are also described for the preparation of phosphinate esters from an alcohol. This novel method provides a convenient and general alternative to more commonly employed conditions such as diazomethane or carbodiimide.

摘要

单取代次膦酸与原硅酸盐酯化反应的产率极高。含亚膦基的酸在这些条件下会选择性地发生反应,而二取代次膦酸和膦酸则保持不变。文中还描述了由醇制备次膦酸酯的一锅法。这种新方法为诸如重氮甲烷或碳二亚胺等更常用的条件提供了一种方便且通用的替代方法。

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Temporary Protection of -Phosphinic Acids as a Synthetic Strategy.作为一种合成策略的次膦酸的临时保护
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Green, Palladium-Catalyzed Synthesis of Benzylic H-phosphinates from Hypophosphorous Acid and Benzylic Alcohols.格林,由次磷酸和苄醇通过钯催化合成苄基次膦酸酯
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Alkylation of H-phosphinate esters under basic conditions.碱性条件下H-次膦酸酯的烷基化反应。
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