The molecular structures of five- and six-membered cyclic sulphonates
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1967/C1/C19670000197
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Nucleophilic Substitution at Different Oxidation States of Sulfur;Progress in Inorganic Chemistry;2007-03-09
2. Ground-state analogs of transition states for attack at sulfonyl, sulfinyl, and sulfenyl sulfur: a sulfuranide dioxide (10-S-5) salt, a sulfuranide oxide (10-S-4) salt, and a sulfuranide (10-S-3) salt;Journal of the American Chemical Society;1985-05
3. Isolation and partial characterization of a covalent intermediate between α-chymotrypsin and o-hydroxy-α-toluenesulfonic acid sultone;Bioorganic Chemistry;1981-06
4. Nucleophilic substitution at sulphur. Part 3. The alkaline hydrolysis of some cyclic and open-chain sulphonate esters;Journal of the Chemical Society, Perkin Transactions 2;1980
5. Hydrolysis enthalpy changes for selected five- and six-membered cyclic esters;Journal of the American Chemical Society;1978-11
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