Stereospecificity in anionic 1, 1‐addition to isocyanides. A re‐examination of the (H− + HNC) potential energy surface
- 1 November 1990
- journal article
- research article
- Published by Wiley in Journal of Physical Organic Chemistry
- Vol. 3 (11) , 697-702
- https://doi.org/10.1002/poc.610031102
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- On the geometry, ionization and dissociation energies of the formyl anion (HCO−)Chemical Physics Letters, 1988
- An MC SCF study of the nucleophilic addition of OH− to ethene and formaldehydeChemical Physics Letters, 1988
- Energy maxima in anionic nucleophilic additions to carbonyl groups: The location of a saddle point for the addition of hydride to formaldehydeCanadian Journal of Chemistry, 1988
- N-aminoisocyanides by 1,1-elimination from formimidoyl chlorideJournal of the Chemical Society, Chemical Communications, 1986
- Stereoelectronic effect in anionic 1,1-addition to isocyanides. An ab initio study of the hydride ion + isocyanic acid systemJournal of the American Chemical Society, 1985
- Self-consistent molecular orbital methods 25. Supplementary functions for Gaussian basis setsThe Journal of Chemical Physics, 1984
- Stereospecific formation of amidines by 1,1-addition of amines to isocyanidesTetrahedron Letters, 1980
- Contribution of triple substitutions to the electron correlation energy in fourth order perturbation theoryThe Journal of Chemical Physics, 1980
- Theoretical study of the reaction of water with the 1,3 dipoles fulminic acid and acetonitrile oxide. Concerted reactions with a proton slide at the transition stateJournal of the American Chemical Society, 1980
- Theoretical models incorporating electron correlationInternational Journal of Quantum Chemistry, 1976