A theoretical approach to the regioselectivity in 1,3‐dipolar cycloadditions of diazoalkanes, hydrazoic acid and nitrous oxide to acetylenes, phosphaalkynes and cyanides
- 5 August 2003
- journal article
- research article
- Published by Wiley in Journal of Physical Organic Chemistry
- Vol. 16 (9), 615-625
- https://doi.org/10.1002/poc.653
Abstract
No abstract availableKeywords
This publication has 83 references indexed in Scilit:
- Orbital Interaction Theory of Organic ChemistryPublished by Wiley ,2000
- Local Softness as a Regioselectivity Indicator in [4+2] Cycloaddition ReactionsThe Journal of Physical Chemistry A, 1997
- Qualitative Valence-Bond Descriptions of Electron-Rich Molecules: Pauling “3-Electron Bonds” and “Increased-Valence” TheoryPublished by Springer Science and Business Media LLC ,1982
- Recent contributions to the mechanism of concerted and non-concerted cycloadditionsPublished by Walter de Gruyter GmbH ,1981
- Orientation in the 1,3-dipolar cycloaddition of diazomethane with alkylethylenesTetrahedron Letters, 1980
- XVII. Spatial Partitioning of Charge DensityIsrael Journal of Chemistry, 1977
- Orientation in the 1,3-dipolar cycloaddition of diazomethane and ethyl vinyl etherThe Journal of Organic Chemistry, 1976
- 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediatesThe Journal of Organic Chemistry, 1976
- Kinetics and Mechanism of 1,3‐Dipolar CycloadditionsAngewandte Chemie-International Edition, 1963
- 1,3‐Dipolar Cycloadditions. Past and FutureAngewandte Chemie-International Edition, 1963