Solvent-Equilibrated Homoadamantyl Chloride Ion Pairs from Chloroformate or Oxachlorocarbene Fragmentations
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, New Brunswick, New Jersey 08903
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol040055w
Reference14 articles.
1. Solvolysis-decomposition of 1-adamantyl chloroformate: evidence for ion pair return in 1-adamantyl chloride solvolysis
2. Solvolysis−Decomposition of 2-Adamantyl Chloroformate: Evidence for Two Reaction Pathways
3. Absolute Kinetics of Alkoxychlorocarbene Fragmentation
4. The Carbene Fragmentation−Ring Expansion Route to Bridgehead Carbocations
5. Solvent-Equilibrated Ion Pairs from Carbene Fragmentation Reactions
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1. Rate and Product Studies with 1-Adamantyl Chlorothioformate under Solvolytic Conditions;International Journal of Molecular Sciences;2021-07-09
2. Synthesis and ring-opening reaction of novel 1,3-dehydroadamantanes possessing phenyl and alkoxyl substituents;Tetrahedron;2013-04
3. Correlation of the Rates of Solvolysis of 1- and 2-Naphthyl Chloroformates Using the Extended Grunwald-Winstein Equation;Bulletin of the Korean Chemical Society;2011-07-20
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