Cyclobutanone-based tandem free radical rearrangements: Formation of bicyclic and tricyclic ketones
- 1 January 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (1) , 39-50
- https://doi.org/10.1016/0040-4020(94)00961-s
Abstract
No abstract availableThis publication has 39 references indexed in Scilit:
- Stereospecific annulation and sequential ring-opening of (R)-carvone: Formation of a novel tricyclic dioneTetrahedron Letters, 1994
- Free radical-based annulation of alkenes yielding fused cycloheptanonesTetrahedron Letters, 1994
- Free radical-mediated ring expansion and related annulationsChemical Reviews, 1993
- Free radical rearrangement of bicyclo[2.2.2]- and bicyclo[4.2.0]octenones systemsTetrahedron, 1993
- Free-radical ring expansion of fused cyclobutanones: stereospecific construction of 5,7-, 6,7-, 7,7-, 8,7-, and 5,8-cis-fused bicyclic systemsThe Journal of Organic Chemistry, 1992
- Novel free radical ring-forming reaction of dichlorocyclobutanones and sequential ring expansionJournal of the American Chemical Society, 1992
- Unusual cyclopropane formation following free radical ring expansionTetrahedron Letters, 1992
- A new free radical-based method for the synthesis of spiroannulated medium ringsTetrahedron Letters, 1992
- Free radical ring expansion of fused cyclobutanones: a new ring expansion annulation stratagemJournal of the American Chemical Society, 1991
- Copper-catalyzed additions of organic polyhalides to olefins: a versatile synthetic toolPublished by Walter de Gruyter GmbH ,1985