Intramolecular Homolytic Substitution Behavior of Acyl Radicals at Sulfur: New Carbonylative Access to γ-Thiolactones
- 1 October 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (22), 7550-7551
- https://doi.org/10.1021/jo971682k
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- α-ketene alkyl and α,β-unsaturated acyl radical intermediates in ring constructionsTetrahedron Letters, 1996
- Rate Constants and Arrhenius Parameters for the Reaction of Acyl Radicals with Bu3SnH and (Me3Si)3SiHOrganometallics, 1995
- Kinetics of intramolecular alkyl radical attack on sulfur in disulfides and thioestersJournal of the Chemical Society, Perkin Transactions 2, 1994
- Regiospecific carbonylation and ring expansion of thietanes and oxetanes catalyzed by cobalt and/or ruthenium carbonylsThe Journal of Organic Chemistry, 1989
- Photolyses of organocobaloximes having aralkyl and (alkylthio)carbonyl groups on the .beta.-position. A radical reaction involving the thioester groupJournal of the American Chemical Society, 1988
- Absolute rate expressions for intramolecular displacement reactions of primary alkyl radicals at sulfurThe Journal of Organic Chemistry, 1987
- Some Extensions of the Reaction of Trivalent Phosphorus Derivatives with Alkoxy and Thiyl Radicals; a New Synthesis of Thioesters1Journal of the American Chemical Society, 1960