65212-15-9Relevant academic research and scientific papers
Organoselenosilane-mediated selective mild access to selenolesters, selenoanhydrides and diacyl diselenides
Capperucci, Antonella,Deglinnocenti, Alessandro,Tiberi, Caterina
experimental part, p. 2248 - 2252 (2011/10/31)
Reaction of acyl chlorides with phenylselenotrimethyl-silane promoted by TBAF afforded a mild general access to selenolesters in good yields. When acyl chlorides were reacted with bis(trimethylsilyl)selenide (HMDSS) in 2:1 or 1:1 ratio a selective entry t
Selenium transfer reaction of primary selenoamides: A novel method for the synthesis of diacylselenides from acyl chlorides
Zhao, Hua-Rong,Zhao, Xin-Jian,Huang, Xian
, p. 3383 - 3387 (2007/10/03)
Diacyl selenides were afford in excent yields by reaction of primary selenoamides with acyl chlorides in chloroform. A possible mechanism is discussed.
Reactions of acyl chlorides with LiAlHSeH. Preparation of diacyl selenides, diacyl diselenides, selenocarboxylates and cyclic selenoanhydrides
Koketsu, Mamoru,Nada, Futoshi,Hiramatsu, Sohma,Ishihara, Hideharu
, p. 737 - 740 (2007/10/03)
Various diacyl selenides, diacyl diselenides and selenocarboxylates were synthesized by reaction of several acyl chlorides with LiAlHSeH. Reaction of diacyl chloride with LiAlHSeH afforded cyclic selenoanhydrides. In the 77Se NMR spectra, we fo
Reactions of O-Silyl Selenocarboxylates; IR and NMR Spectra of Heteroatom-substituted Selenocarboxylates
Kageyama, Hideki,Kido, Kenji,Kato, Shinzi,Murai, Toshiaki
, p. 1083 - 1088 (2007/10/02)
O-Silyl selenocarboxylates 1 react readily with acyl chlorides to give selenoanhydrides.Attempts to synthesize unsymmetrical selenoanhydrides selectively gave mixtures of the desired products with symmetrical selenoanhydrides.Ph3GeCl, Ph3SnCl, Ph3PbCl, Ph
