Preparation of 2-Arylethynylselanylacetonitriles from 4-Aryl-1,2,3-selenadiazoles
摘要:
Base decomposition of 4‐(substituted phenyl)‐1,2,3‐selenadiazoles at room temperature resulted in 2‐(substituted phenyl)‐ethynylselenolate anions, which were immediately reacted with bromoacetonitrile to give a series of 2‐(substituted phenyl)ethynylselanylacetonitriles.
Laishev, V. Z.; Petrov, M. L.; Petrov, A. A., Journal of Organic Chemistry USSR (English Translation), 1982, vol. 18, p. 450 - 454
作者:Laishev, V. Z.、Petrov, M. L.、Petrov, A. A.
DOI:——
日期:——
A Facile Synthesis of<i>N</i>-(4-Aryl-1,3-dithiol-2-ylidene)-amides,<i>N</i>-(4- or 5-Aryl-1,3-thiaselenol-2-ylidene)-amides, and<i>N</i>-(4-Aryl-1,3-diselenol-2-ylidene)-amides
作者:A. Shafiee、G. Fanaii
DOI:10.1055/s-1984-30887
日期:——
Synthesis and radioprotective effects of derivatives of thiadiazoles, dithiolidenes, and their selenium analogs
作者:L. L. Petrova、L. V. Trufanova、M. L. Petrov、M. A. Abramov、N. I. Zmitrovich、N. A. Terent'eva
DOI:10.1007/bf02220017
日期:1994.2
Ganjian, I.; Lalezari, I.; DiMeo, S.V., Journal of Heterocyclic Chemistry, 1986, vol. 23, # 3, p. 893 - 895