30038-29-0Relevant academic research and scientific papers
Mono- and Di(dechloromethylthioylation) of Dichloromethylarenes with S-Methyl Diethylthiophosphinate
Gazizov,Valieva,Ivanova, S. Yu.,Khairullin,Kirillina, Yu. S.,Antipin
, p. 257 - 260 (2019/12/25)
Abstract: The attack of the thiol sulfur atom (P–SMe) on the methine carbon as the main route of the new reaction of dichloromethylarenes with S-methyl diethylthiophosphinate has been predicted and experimentally confirmed on the basis of the electronic s
Reactions of Benzylidene Chlorides with S-Methyl Diethylphosphinothioate
Gazizov,Valieva,Ivanova, S. Yu.,Karimova,Khairullin,Gazizova
, p. 2386 - 2389 (2020/02/25)
S-Methyl diethylphosphinothioate reacted with benzylidene chlorides to give the corresponding aryl(chloro)methyl methyl sulfide and diethylphosphinoyl chloride. The product structure suggests initial attack of the methylsulfanyl group on the CH carbon ato
S-Methyl diethylthiophosphinate in mono- and di(dechloromethylthioylation) of substituted benzylidene chlorides
Gazizov,Valieva,Ivanova, S. Yu.,Khairullin,Kirillina, Yu. S.,Khairullina,Ibragimov, Sh. N.
, p. 1889 - 1892 (2019/10/22)
The main route of a new reaction of (dichloromethyl)arenes with S-methyl diethylthiophosphinate is the attack of the thiol sulfur atom (P–SMe) on the methylene carbon atom. A new method for synthesizing dimethyl dithioacetals of arenecarbaldehydes without
An indium-TMSCl promoted reaction of diphenyl diselenide and diorganyl disulfides with aldehydes: novel routes to selenoacetals, thioacetals and alkyl phenyl selenides
Ranu, Brindaban C.,Saha, Amit,Mandal, Tanmay
experimental part, p. 2072 - 2078 (2009/07/11)
The reactions of diphenyl diselenide and dialkyl disulfides with aldehydes in the presence of In-TMSCl have been investigated. Aliphatic aldehydes provide the corresponding selenoacetals and aromatic aldehydes lead predominantly to benzyl phenyl selenides
SYNTHESIS OF 5-ARYL- AND 5-ALKYL-4-ETHOXYCARBONYL-2-METHYLTHIO-1,3-THIAZOLES FROM DIMETHYL N-(ETHOXY-CARBONYLMETHYL)IMINODITHIOCARBONATE AND DITHIOESTERS
Alonso, G.,Alvarez-Ibarra, C.,Orellana, G.,Quiroga, M. L.
, p. 215 - 220 (2007/10/02)
In this paper we give account of an efficient synthesis of 5-aryl- and 5-alkyl-4-ethoxycarbonyl-2-methylthio-1,3-thiazoles from dimethyl N-(ethoxycarbonylmethyl)iminodithiocarbonate and dithioesters.
Electroreduction of Organic Compounds, 9. - Convenient Electrochemical Preparation of Thioacetals from Dithioesters
Drosten, Gisela,Mischke, Peter,Voss, Juergen
, p. 1757 - 1762 (2007/10/02)
Thioacetals are obtained as main products on electroreduction of alkyl dithiocarboxylates of various types in the presence of dimethyl sulfate in methanol. (Z)- and (E)-1,2-diaryl-1,2-bis(methylthio)ethenes are formed as byproducts.No reduction to form be
