Heterocyclic thiones and their analogs in 1,3-dipolar cycloaddition reactions: IV. Reactions of 4-aryl-2-phenyl-1,2-dihydrophthalazine-1-thiones with nitrile imides

E. V. Budarina; V. F. Plotnikov; N. N. Labeish; V. K. Bel'skii; V. A. Galishev

Journal Article

Heterocyclic thiones and their analogs in 1,3-dipolar cycloaddition reactions: IV. Reactions of 4-aryl-2-phenyl-1,2-dihydrophthalazine-1-thiones with nitrile imides

Budarina E
Plotnikov V
Labeish N
et al.

Russian Journal of Organic Chemistry (2005) 41(3) 455-460

DOI: 10.1007/s11178-005-0187-x

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Abstract

4-Aryl-2-phenyl-1,2-dihydrophthalazine-1-thiones react with nitrile imides according to the [3 + 2]-cycloaddition pattern to give phthalazinespirothiadiazoles. The reaction occurs regioselectively at the exocyclic C=S bond. © 2005 Pleiades Publishing, Inc.

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Budarina, E. V., Plotnikov, V. F., Labeish, N. N., Bel’skii, V. K., & Galishev, V. A. (2005). Heterocyclic thiones and their analogs in 1,3-dipolar cycloaddition reactions: IV. Reactions of 4-aryl-2-phenyl-1,2-dihydrophthalazine-1-thiones with nitrile imides. Russian Journal of Organic Chemistry, 41(3), 455–460. https://doi.org/10.1007/s11178-005-0187-x

Heterocyclic thiones and their analogs in 1,3-dipolar cycloaddition reactions: IV. Reactions of 4-aryl-2-phenyl-1,2-dihydrophthalazine-1-thiones with nitrile imides

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