Synthesis of phosphorus-substituted dialkylamides of organophosphorus acids, containing P–C–N–P moiety
✍ Scribed by Andrey A. Prishchenko; Mikhail V. Livantsov; Olga P. Novikova; Ludmila I. Livantsova; Valery S. Petrosyan
- Book ID
- 102231980
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 257 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20468
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✦ Synopsis
Abstract
Reactions of N‐(trimethylsilyl)amino‐methylphosphonates with organophosphorus acid chlorides were studied, which allowed to develop convenient synthetic approaches to novel phosphorus‐substituted dialkylamides of organophosphorus acids, including a P–C–N–P moiety. Certain properties of the resulting compounds are presented. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:495–499, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20468
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The dependence of the protolytic decomposition rate of triphenylmethylphosphonous dichloride 1 was allowed to react with 3 equivalents of HTMG, forming the stable phosphorus amides on the substituents at phosphorus is decribed. On treatment with HCl, the NЈ,NЈ,NЉ,NЉ-phosphonium salt 19, soluble in w