A convenient preparation of symmetrical and unsymmetrical 1,2-diketones: application to fluorinated phenytoin synthesis
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (35) , 7265-7274
- https://doi.org/10.1016/s0040-4020(01)88265-x
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- The metabolism of 2- and 4-fluoro-17β- oestradiol in the rat and its implications for oestrogen carcinogenesisBiochemical Pharmacology, 1992
- Regioselective synthesis of a-ring halogenated derivatives of 17α-ethynyloestradiolTetrahedron, 1991
- Efficient regioselective a-ring functionalization of oestrogensTetrahedron, 1990
- A new facile synthesis of α-dicarbonyl compounds by oxidation of alkynes with Mo(VI) peroxocomplex promoted by mercuric acetateTetrahedron Letters, 1986
- A convenient “one-pot” synthesis of epoxy alcohols via photooxygenation of olefins in the presence of titanium(IV) catalystTetrahedron Letters, 1986
- A versatile access to unsymmetrical and symmetrical α-diketones via organotin reagentsTetrahedron Letters, 1985
- A very efficient preparation of 1,2-diketonesTetrahedron Letters, 1985
- Reactions of acyl anions generated from acid chlorides and diiodosamariumTetrahedron Letters, 1984
- Umwandlung von α-aminosäuren in α-diketone über oxazolin-zwischenstufenTetrahedron Letters, 1983
- Insertion of carbon monoxide into carbon-lithium bonds. A convenient one-step synthesis of 1,2-diketone diaryl derivativesThe Journal of Organic Chemistry, 1982