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Synthesis 2010(18): 3113-3116
DOI: 10.1055/s-0030-1258179
DOI: 10.1055/s-0030-1258179
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New YorkHydrophosphonylation of Benzoylhydrazones Using Iodine as a Catalyst: A Facile Synthesis of α-(N′-Acylhydrazino)-Substituted Phosphonates [¹]
Further Information
Received
5 May 2010
Publication Date:
16 July 2010 (online)
Publication History
Publication Date:
16 July 2010 (online)
Abstract
A simple and efficient method for the synthesis of α-(N′-acylhydrazino)-substituted phosphonates has been developed using the hydrophosphonylation of benzoylhydrazones with triethyl phosphite in the presence of iodine as a catalyst at room temperature. The products are formed in excellent yields (89-95%) within two to three hours.
Key words
hydrophosphonylation - benzoylhydrazones - triethyl phosphite - α-(N′-acylhydrazino)-substituted phosphonates - iodine
Part 205 in the series ‘Studies on Novel Synthetic Methodologies’.
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Part 205 in the series ‘Studies on Novel Synthetic Methodologies’.