Synthesis of 3,3,4,4,5-pentasubstituted-5-vinyl-4,5-dihydro-3H-pyrazoles: Route to vinylcyclopropanes

DOI: 10.1515/HC.2006.12.5.337

Source and publish data:

Heterocyclic Communications p. 337 - 340 (2006)

Update date:2022-08-03

Topics:

Authors:

Towns, Kishia K.

Vasquez, Pedro C.

Kennedy, G. Davon

Baumstark

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Article abstract of DOI:10.1515/HC.2006.12.5.337

The reaction of vinyl-substituted-3,4-dihydro-2H-pyrazoles, 1a (R=Ph) and b (R=Me) [synthesized by reaction of vinyllithium with the corresponding cyclic azines], with iodobenzene diacetate produced the vinyl substituted-4,5-dihydro- 3H-pyrazoles, pyrazol

Full text of DOI:10.1515/HC.2006.12.5.337

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Article Doi

Synthesis of 3,3,4,4,5-pentasubstituted-5-vinyl-4,5-dihydro-3H-pyrazoles: Route to vinylcyclopropanes

DOI: 10.1515/HC.2006.12.5.337

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Authors:

Article abstract of DOI:10.1515/HC.2006.12.5.337

Full text of DOI:10.1515/HC.2006.12.5.337

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