Theoretical kinetic and thermodynamic studies of the strain energies and ring size effects of the 1,3-dipolar cycloaddition reactions on ethinamate medicine analogs

Author:

Hashemi Marzieh,Taherpour Avat (Arman)

Funder

Theoretical and Computational Research Center of Chemistry Faculty

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference82 articles.

1. Synthetic Applications of 1, 3-dipolar Cycloaddition Chemistry toward Heterocycles and Natural Products;Padwa,2003

2. N2 elimination thermolysis reactions of 9-(4-and 5-substituted-1, 2, 3-triazol-1-yl) acridines to produce 1H-pyrido-[4, 3, 2-kl] derivatives–A theoretical study;Taherpour;Chem. Phys. Lett.,2017

3. Theoretical study of 1, 3-dipolar reactions of myrcene and trimethylsilylazide;Taban;Lett. Org. Chem.,2017

4. 1, 3-dipolar cycloadditions. Past and future;Huisgen;Angew Chem. Int. Ed. Engl.,1963

5. Kinetics and mechanism of 1, 3-dipolar cycloadditions;Huisgen;Angew Chem. Int. Ed. Engl.,1963

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