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Synlett 2010(10): 1477-1480
DOI: 10.1055/s-0029-1220072
DOI: 10.1055/s-0029-1220072
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
An Efficient Synthesis of Highly Functionalized 4H-Pyrano[3,2-d]isoxazoles via Isocyanide-Based Three-Component Reaction
Further Information
Received
23 March 2010
Publication Date:
26 May 2010 (online)
Publication History
Publication Date:
26 May 2010 (online)

Abstract
We present a novel, convenient, and efficient method for synthesizing polysubstituted 4H-pyrano[3,2-d]isoxazoles based on a three-component reaction. The zwitterions generated from the reaction of isocyanides and dialkyl acetylenedicarboxylates are reacted with 3-phenylisoxazol-4-(5H)-one to produce the title compounds in good yield.
Key words
4H-pyrano[3,2-d]isoxazole - isocyanides - 3-phenylisoxazol-4-(5H)-one - three-component reactions - acetylenic esters
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