Journal article
Reactions of γ-acyloxy-β-ketophosphonates: New routes to 3(2h)- and 2(3h)-dihydrofuranones
Tetrahedron letters, Vol.25(40), pp.4467-4470
1984
DOI: 10.1016/S0040-4039(01)81468-4
Abstract
Depending on the reaction conditions, γ-acyloxy-β-ketophosphonate anions can undergo either an intramolecular Wittig-like condensation or an unexpected rearrangement which affords an enol ester product.
Details
- Title: Subtitle
- Reactions of γ-acyloxy-β-ketophosphonates: New routes to 3(2h)- and 2(3h)-dihydrofuranones
- Creators
- Gary J DrtinaPaul SampsonDavid F Wiemer
- Resource Type
- Journal article
- Publication Details
- Tetrahedron letters, Vol.25(40), pp.4467-4470
- Publisher
- Elsevier Ltd
- DOI
- 10.1016/S0040-4039(01)81468-4
- ISSN
- 0040-4039
- eISSN
- 1873-3581
- Language
- English
- Date published
- 1984
- Academic Unit
- Chemistry; Neuroscience and Pharmacology
- Record Identifier
- 9983985936602771
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