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Synthesis 2010(20): 3504-3508
DOI: 10.1055/s-0030-1257889
DOI: 10.1055/s-0030-1257889
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of a Novel Class of β-Lactam Derivatives of 1-Aminophosphonates by Staudinger Ketene-Imine [2+2]-Cycloaddition Reaction
Further Information
Received
31 May 2010
Publication Date:
22 July 2010 (online)
Publication History
Publication Date:
22 July 2010 (online)
Abstract
A novel class of β-lactam derivatives of 1-aminophosphonates was synthesized by Staudinger [2+2] cycloaddition reaction of ketenes with imines derived from 1-aminophosphonates. Treatment of aromatic aldehydes with ammonia and diethyl phosphite followed by a reaction with ketenes, which are generated from the appropriate acid chloride and a tertiary amine, gave a novel class of β-lactam derivatives of 1-aminophosphonates. The major or, in some cases, sole product of the cycloaddition is the cis-β-lactam.
Key words
1-aminophosphonates - β-lactams - ketenes - imines - [2+2]-cycloaddition reaction
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