Transition State Polarization Effects and Steric Effects in the Kinetics of Alkoxycarbonyl-Substituted Radical Fragmentations
- 1 July 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (30) , 7147-7148
- https://doi.org/10.1021/ja971141c
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Infrared laser transient absorption spectroscopy of the ethyl radicalThe Journal of Chemical Physics, 1996
- Mechanism of Action of Vitamin B12. A New Test for Free Radical Intermediates Using a Cyclopropane Model for the Methylmalonyl-CoA to Succinyl-CoA Carbon Skeleton RearrangementJournal of the American Chemical Society, 1996
- Direct Measurements of Unimolecular Radical Kinetics Employing Ultrafast Radical Rearrangements as ReportersJournal of the American Chemical Society, 1996
- Absolute Rate Constants for the Addition of Methyl Radicals to Alkenes in Solution: New Evidence for Polar InteractionsJournal of the American Chemical Society, 1996
- α-Ethoxycarbonyl and α-methoxy substituted radical clocksTetrahedron Letters, 1995
- Ultrafast studies of photochromic spiropyrans in solutionJournal of the American Chemical Society, 1992
- Raw Materials and Energy: A Challenge for Polymer ResearchAngewandte Chemie International Edition in English, 1983
- The Structure of Diskatole1The Journal of Organic Chemistry, 1961