ADDITIONS OF 5-PHENYLTETRAZOLE AND OTHER HETEROCYCLIC NH COMPOUNDS TO OLEFINS

Авторы

  • Alan R. Katritzky Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720
  • Ming Qi Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720
  • Adam P. Wells Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-720

Аннотация

The reactivity of a range of heterocyclic NH compounds toward cyclohexene under p-toluenesulfonic acid catalysis was surveyed. 1 ,2,4- Тгiаzоlе (38%), carbazole (67%) and 5-phenyltеtrazolе (83%) gave significant amounts of addition products. 5-Phenyltetrazole reacts with a wide range of unactivated olefins, to give addition products in 65% to 90% yield. This method represents a general, preparatively useful route to 2-alkyl-5-phеnyltеtrazoles.

How to Cite
Katritzky, A. R.; Qi, M.; Wells, A. P. Chem. Heterocycl. Compd. 1996, 32, 1305. [Khim. Geterotsikl. Soedin. 1996, 1520.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169962

Загрузки

Опубликован

1996-11-23

Выпуск

№ 11/12 (1996)

Раздел

Оригинальные статьи