Synchronous or Asynchronous? An “Experimental” Transition State from a Direct Comparison of Experimental and Theoretical Kinetic Isotope Effects for a Diels−Alder Reaction
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (41) , 9984-9985
- https://doi.org/10.1021/ja9615278
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- DFT study of the Diels–Alder reactions between ethylene with buta-1,3-diene and cyclopentadieneJournal of the Chemical Society, Perkin Transactions 2, 1995
- Density functional transition states of organic and organometallic reactionsThe Journal of Chemical Physics, 1994
- Ab initio Cs transition state for the Diels-Alder reaction of acetylene and butadieneThe Journal of Organic Chemistry, 1990
- Substituent effects and transition structures for Diels-Alder reactions of butadiene and cyclopentadiene with cyanoalkenesJournal of the American Chemical Society, 1989
- Transition-state structure variation in the Diels-Alder reaction from secondary deuterium kinetic isotope effects. The reaction of nearly symmetrical dienes and dienophiles is nearly synchronousJournal of the American Chemical Society, 1989
- Synchronicity in Multibond ReactionsAnnual Review of Physical Chemistry, 1988
- Mechanism of the Diels-Alder reaction. Studies of the addition of maleic anhydride to furan and methylfuransJournal of the American Chemical Society, 1984
- Endo preference in the Diels-Alder cycloaddition of butadiene and maleic anhydrideThe Journal of Organic Chemistry, 1982
- The Secondary Deuterium Isotope Effect on the Diels-Alder ReactionJournal of the American Chemical Society, 1964
- The Mechanism of a Diels-Alder ReactionJournal of the American Chemical Society, 1963