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Synthesis and oxidative rearrangement of selenenylated dihydropyrans
Author(s) -
Sébastien Redon,
Xavier Pannecoucke,
Xavier Franck,
Françis Outurquin
Publication year - 2008
Publication title -
organic and biomolecular chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.923
H-Index - 146
eISSN - 1477-0539
pISSN - 1477-0520
DOI - 10.1039/b718825k
Subject(s) - oxidative phosphorylation , contraction (grammar) , tetrahydrofuran , chemistry , sigmatropic reaction , stereochemistry , organic chemistry , philosophy , linguistics , biochemistry , solvent
Selenenylated dihydropyrans prepared by inverse demand hetero-Diels-Alder reactions undergo oxidative rearrangement when treated with H(2)O(2), leading to tetrahydrofuran-2-ones by ring contraction.

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