Reactions of Tin(IV) Enolates and Radicals Derived from the Tin Hydride Scission of Cyclopropyl Ketones
- 1 August 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (16) , 5248-5249
- https://doi.org/10.1021/jo970914c
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Fragmentation-cyclization reactions of O-stannyl ketyls: The synthesis of an angular triquinane skeletonTetrahedron Letters, 1996
- Tin(IV) enolates from allylic O-stannyl ketyls: Reactions with alkyl halides and HMPATetrahedron Letters, 1996
- Construction of a linear triquinane skeleton by an O-stannyl ketyl radical rearrangementChemical Communications, 1996
- Intermolecular aldol reactions via allylic o-stannyl ketylsTetrahedron Letters, 1995
- α-ketocyclopropane ring-opening reactions via o-stannyl ketylsTetrahedron Letters, 1995
- Cyclization Reactions of Allylic O-Stannyl KetylsThe Journal of Organic Chemistry, 1995
- Free Radical Approach to Directed Aldol-Type Reactions Promoted by Allylic O-Stannyl KetylsThe Journal of Organic Chemistry, 1995
- Free radical cyclizations promoted by allylic O-stannyl ketyls: the intramolecular coupling of the .beta.-carbons of activated alkenesJournal of the American Chemical Society, 1991
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2Synthesis, 1988
- Radical reactions in organic synthesisTetrahedron, 1987