Rates of base-catalyzed hydrogen exchange of terminal acetylenes in aqueous solution. Absence of a resonance interaction
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00356a011
Cited by 12 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. Reactivity of a Germene toward Terminal Alkynes: Competition between Cycloaddition, Ene-Addition, and CH-Insertion;Organometallics;2011-03-24
2. A New Approach to Analysis of the Nonlinearity of the Brönsted Relationship: III An Empirical Procedure Combining the Method of Correlations and the Concept of Hard and Soft Acids and Bases, as Applied to Normal CH Acids;Russian Journal of General Chemistry;2004-07
3. Kinetic isotope effects in hydrogen exchange of aromatic CH bonds in benzene, fluorobenzene, and nitrogen-containing heterocycles with solution of alkali metal amide in liquid ammonia;Russian Journal of General Chemistry;2001
4. Proton Transfer from the C5-proR/proS Positions of l-Dihydroorotate: General-Base Catalysis, Isotope Effects, and Internal Return1;Journal of the American Chemical Society;1999-12-01
5. Normal acid/base behaviour in proton transfer reactions to alkoxy substituted carbenes: estimates for intrinsic barriers to reaction and pK(a) values;CAN J CHEM;1999
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