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Synthesis and oxidative rearrangement of selenenylated dihydropyrans.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2008 Apr 07; Vol. 6 (7), pp. 1260-7. Date of Electronic Publication: 2008 Feb 27. - Publication Year :
- 2008
-
Abstract
- 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.
Details
- Language :
- English
- ISSN :
- 1477-0520
- Volume :
- 6
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18362967
- Full Text :
- https://doi.org/10.1039/b718825k