Ab Initio Theoretical Studies on the Ring-Opening Modes of the Oxiranyl-, Aziridinyl-, Oxaziridinyl-, and Thiaranylmethyl Radical Systems
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9505942
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2. Novel synthesis of vinyl ethers induced by carbon–halogen bond homolysis
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4. Radical reactions of epoxides. 2. intramolecular competition between cyclopropylmethyl and oxiranylmethyl radical ring-opening rearrangements
5. Calibration of a new horologery of fast radical clocks. Ring-opening rates for ring- and .alpha.-alkyl-substituted cyclopropylcarbinyl radicals and for the bicyclo[2.1.0]pent-2-yl radical
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