Phenolysis ofexo- andendo-2-Norbornylp-Toluenesulfonates. Rates and Product Distributions
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/46/9/46_9_2905/_pdf
Reference14 articles.
1. Neighboring Carbon and Hydrogen. X. Solvolysis of endo-Norbornyl Arylsulfonates1,2,3
2. Neighboring Carbon and Hydrogen. XI. Solvolysis of exo-Norbornyl p-Bromobenzenesulfonate1,2,3
3. The Nonclassical Norbornyl Cation1
4. Substituent Effects on 2-Norbornyl Solvolysis Rates. The 6,6-Dimethyl Group1
5. Solvolyse von Toluolsulfonsäureestern, XXIV. Norborneole
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1. Non-Catalyzed C-Alkylation of Phenols With Cyclic Secondary Alkyl Bromides;Synthetic Communications;1996-11
2. Acid-Catalyzed Hydrolysis of Bridged Bi- and Tricyclic Compounds. XXVII. An Application of the Excess Acidity Method to the Norbornyl Cation Problem.;Acta Chemica Scandinavica;1989
3. REACTION OFexo-2-NORBORNYL AND 1-ADAMANTYLp-TOLUENESULFONATES WITH SODIUM PHENOXIDE IN TETRAHYDROFURAN. IONIZATION OF THE SUBSTRATES UNDER “APPARENTLY-SN2” CONDITIONS;Chemistry Letters;1981-07-05
4. Phenolyses of 1-aryl-1-methylethyl p-nitrobenzoates and some simple alkyl systems: characteristic features of phenol as a solvolytic solvent;Journal of the Chemical Society, Perkin Transactions 2;1977
5. Retentive solvolysis. Part X. Retentive solvolysis of optically active para-substituted 1-phenylethyl p-nitrobenzoates in phenolic solvents: rate, steric course, product distribution, and mechanism;Journal of the Chemical Society, Perkin Transactions 2;1975
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