87356-38-5Relevant academic research and scientific papers
Photoreductive cleavage of Phenyl-Selenium Bonds of Phenylselenoalkanes.
Ferritto, Rafael,Vogel, Pierre
, p. 1193 - 1196 (2007/10/02)
Photo-induced-electron transfer from triethylamine to phenylselenoalkanes can lead to selective reduction and cleavage of the Ph-Se bond leading to the formation of benzene and the corresponding alkylselenyl radicals that dimerize.
Synthesis of Functionalised Heterocyclic Selenoamide Derivatives and Their Reactions
Singh, Harjit,Malhotra, Nageshwar
, p. 328 - 330 (2007/10/02)
Sodium pyridyl (8b)/isoquinolinyl (8c) selenates on treatment with ethyl chloroacetate give ethyl 2,2'-diselenobis(acetate) (9) and the corresponding carboxamides, but sodium quinazolinylselenate (8a) forms ethyl 2-(4-quinazolinylseleno)acetate (6a) and ethyl 2-acetate (12).With chloroacetonitrile, 8a-c form condensed mesoionic selenazoles, 3-aminoselenazolequinazolin-4-ium hydroxide inner salt (14a), 3-aminoselenazolepyridinium hydroxide inner salt (14b) and 3-aminoselenazoleisoquinolinium hydroxide inner salt (14c) respectively.
