Thermally controlled decarboxylative [4 + 2] cycloaddition between alkoxyoxazoles and acrylic acid: expedient access to 3-hydroxypyridines. - Archive ouverte HAL Access content directly
Journal Articles Organic Letters Year : 2013

Thermally controlled decarboxylative [4 + 2] cycloaddition between alkoxyoxazoles and acrylic acid: expedient access to 3-hydroxypyridines.

Abstract

A modified Kondrat'eva cycloaddition involving an unprecedented thermally controlled metal-free decarboxylative aromatization affords an expedient access to natural 3-hydroxypyridine/piperidine systems.
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hal-00996416 , version 1 (26-05-2014)

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Laurie-Anne Jouanno, Vincent Tognetti, Laurent Joubert, Cyrille Sabot, Pierre-Yves Renard. Thermally controlled decarboxylative [4 + 2] cycloaddition between alkoxyoxazoles and acrylic acid: expedient access to 3-hydroxypyridines.. Organic Letters, 2013, 15 (10), pp.2530-2533. ⟨10.1021/ol4010195⟩. ⟨hal-00996416⟩
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