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Synthesis of new phosphonato esters by reaction between triphenyl or trialkyl phosphite and acetylenic diesters in the presence of NH-containing compounds

✍ Scribed by Ghasem Marandi; Malek Taher Maghsoodlou; Nourallah Hazeri; Reza Heydari; Sayyed Mostafa Habibi-Khorassani; Niloufar Akbarzadeh Torbati; Seyed Sajad Sajadikhah; Danial Saravani; Mansoureh Rakhshanipour; Samira Gholamipour; Faramarz Rostami-Charati; Brian W. Skelton; Mohamed Makha; Zeynab Zare; Mojtaba Lashkari

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 193 KB
Volume: 22
Category: Article
ISSN: 1042-7163
DOI: 10.1002/hc.20725

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✦ Synopsis

Abstract

The reaction between triphenyl or trialkyl phosphite and acetylenic esters in the presence of some heterocyclic or aromatic NH compounds such as thiazolidine‐2,4‐dione, 2‐methyl indole, 5‐bromoisatine, 3‐nitroacetanilide, saccharin, 5,5‐dimethylhydantoin, 2‐nitroaniline, 4‐nitroaniline, benzophenon hydrazine, and anthranilic acid led to the formation of phosphonato esters in high yield. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:630–639, 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20725

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