Kinetic Studies of Solvolysis. XVI. Phenolysis ofcis- andtrans-4-t-Butylcyclohexyp-Toluenesulfonates. Rates and Product Distribution
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference26 articles.
1. Kinetic Studies of Solvolysis. XI. The Steric Course of the Phenolyses of Optically Active α-Phenylethyl Chloride in Mixtures of Various Phenols and Organic Solvents—A Mechanism for the SN1 Reaction with a Net Retention of Configuration
2. A Retentive SN1 Hydrolysis in Aqueous Acrylonitrile and the Polymerization of Acrylonitrile Initiated by the SN1 Hydrolysis Intermediate
3. Kinetic Studies of Solvolysis. XIII. The Solvolyses of Optically-active α-Phenylethyl Chloride in Binary Mixtures of Phenol and Water—The SN1 Hydrolysis with the Retention of the Configuration
4. Kinetic Studies of Solvolysis. XIV. The Solvolysis of Optically Active α-Phenylethyl Chloride in Binary Mixtures of Methanol and Phenol —The SN1 Methanolysis with the Retention of the Configuration—
5. Neighboring Carbon and Hydrogen. XIX. t-Butylcyclohexyl Derivatives. Quantitative Conformational Analysis
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3. Solvolysis in Carboxamides. II. Solvolytic Elimination of 7β-Methylbicyclo[3.3.1]non-3β-yl Tosylate in Carboxamides;Bulletin of the Chemical Society of Japan;1978-02
4. The stereochemistry of fragmentation products formed in the lead tetraacetate and related oxidations of alcohols. Part. I. ?-fragmentation ofcis-andtrans-4-t-Butylcyclohexanemethanol;Helvetica Chimica Acta;1974-04-27
5. Solvolyses of axial and equatorial epimers of trans-2-decalyl tosylate and their 6-keto and 6-keto-.DELTA.5(10) derivatives;The Journal of Organic Chemistry;1973-08
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