Rearrangement of 2-Dienylcyclobutenones. Synthesis of Highly Substituted Annulated Furans
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (8) , 2584-2585
- https://doi.org/10.1021/jo952247y
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Stereocontrolled Synthesis of 3-Acyl-4-alkoxy-5-aryl-1,2,4(E)-pentatrienes and Their Subsequent Electrocyclization to NaphthalenesThe Journal of Organic Chemistry, 1995
- Regioselective Synthesis of Highly Substituted NaphtholsThe Journal of Organic Chemistry, 1995
- Synthesis of substituted cyclobutenediones from 3-ethenyl-4-methoxy-cyclobutene-1,2-dioneTetrahedron Letters, 1991
- Rearrangements of cyclobutenones. Synthesis of benzoquinones from 4-alkenyl-4-hydroxycyclobutenonesJournal of the American Chemical Society, 1990
- Photolysis of 4-substituted-4-hydroxy-3-cyclobuten-1-ones: a new route to butenolides from 4-hydroxycyclobutenonesTetrahedron Letters, 1988
- An improved method for the synthesis of substituted cyclobutenedionesThe Journal of Organic Chemistry, 1988
- A general, regiospecific synthesis of highly substituted quinonesThe Journal of Organic Chemistry, 1986
- Synthesis of benzoquinones and annulated derivatives from conjugated ketenesThe Journal of Organic Chemistry, 1986
- Theory of stereoselection in conrotatory electrocyclic reactions of substituted cyclobutenesJournal of the American Chemical Society, 1985