4.7 Article

An improved route to the synthetic of diphenyl α-(diethoxythiophosphorylamino) methylphosphonates

Journal

BIOORGANIC CHEMISTRY
Volume 34, Issue 4, Pages 167-172

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2006.05.003

Keywords

Mannich type reaction; thiophosphate-phosphonate derivatives; acetyl chloride; X-ray crystal structure

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An improved method for the synthesis of Diphenyl alpha-(diethoxythiophosphorylamino)methylphosphonates under mild conditions is described. It consists of the reaction of diethyl thiophosphoramidate (1) with triphenyl phosphite (3) and a substituted benzylaldehyde or ketone (2) by a one-pot procedure with the aid of acetyl chloride. (c) 2006 Elsevier Inc. All rights reserved.

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