[2+2+2]-Cycloreversion reactions: a theoretical elucidation of thermodynamic and through-bond coupling effects on activation energies †‡
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1999/P2/A904536H
Cited by 24 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. Theoretical Analysis of the Fragmentation of (CO)5: A Symmetry-Allowed Highly Exothermic Reaction that Follows a Stepwise Pathway;The Journal of Organic Chemistry;2015-09-16
2. Theoretical studies on [2 + 2 + 2] reaction mechanisms of three ethynes. More accurate estimation of activation energy;Journal of Physical Organic Chemistry;2013-05-05
3. Why Nature Eschews the Concerted [2 + 2 + 2] Cycloaddition of a Nonconjugated Cyanodiyne. Computational Study of a Pyridine Synthesis Involving an Ene–Diels–Alder–Bimolecular Hydrogen-Transfer Mechanism;The Journal of Organic Chemistry;2012-01-25
4. The [2 + 2 + 2] mechanisms of trimerization of three ethynes and monosilaethylenes;Theoretical Chemistry Accounts;2011-06-23
5. ChemInform Abstract: [2 + 2 + 2]-Cycloreversion Reactions: A Theoretical Elucidation of Thermodynamic and Through-Bond Coupling Effects on Activation Energies.;ChemInform;2010-06-10
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