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Synthesis 2004(5): 668-670
DOI: 10.1055/s-2004-815978
DOI: 10.1055/s-2004-815978
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Nitrated Thienylphosphonates via Michaelis-Arbuzov-Type Rearrangement
Further Information
Received
6 January 2004
Publication Date:
19 February 2004 (online)
Publication History
Publication Date:
19 February 2004 (online)
Abstract
A facile, catalyst-free synthesis of diethyl thienylphosphonates under mild conditions without solvent is described. The desired products were obtained, via a Michaelis-Arbuzov-type rearrangement, from various activated thienyl halides by reacting with triethyl phosphite.
Key words
Michaelis-Arbuzov rearrangement - phosphorus - heterocycles - thienylphosphonates - halides
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