106576-52-7Relevant academic research and scientific papers
Synthesis of new 3-substituted 1,3-oxazolidine-2-thiones
Takibayeva,Ibraev,Kabieva
, (2017)
Reaction of N-alkylsubstituted ethanolamines with carbon disulfide followed by reaction with benzoyl chloride afforded N-substituted oxazolidine-2-thiones.
Ruthenium-Catalyzed O- to S-Alkyl Migration: A Pseudoreversible Barton-McCombie Pathway
Mahy, William,Plucinski, Pawel,Jover, Jesús,Frost, Christopher G.
supporting information, p. 10944 - 10948 (2015/09/15)
A practical ruthenium-catalyzed O- to S-alkyl migration affords structurally diverse thiooxazolidinones in excellent yields. Our studies suggest this catalytic transformation proceeds through a pseudoreversible radical pathway drawing mechanistic parallels to the classic Barton-McCombie reaction. A radical step in a new direction: A practical ruthenium-catalyzed O- to S-alkyl migration affords structurally diverse thiooxazolidinones in excellent yields. Experimental and computational studies suggest a pseudoreversible radical pathway drawing mechanistic parallels to the classic Barton-McCombie reaction.
Spectroscopic Identification of 3-Substituted 4-Methoxycarbonyl-1,3-thiazolidine (or -oxazolidine)-2-thiones and 2-Substituted Thio-4-methoxycarbonyl-Δ2-1,3-thiazolines (or -oxazolines)
Nagao, Yoshimitsu,Inoue, Keiko,Yamaki, Masae,Shiro, Motoo,Takagi, Shuzo,Fujita, Eiichi
, p. 4293 - 4300 (2007/10/02)
rac-4-Methoxycarbonyl-Δ2-1,3-thiazoline 2a-z and rac-4-methoxycarbonyl-1,3-thiazoline-2-thiones 3a,d-t were examined by carbon-13 and proton nuclear magnetic resonance and ultraviolet spectroscopic methods to provide a basis for spectroscopic i
Reaction of Tri-n-butyltin ω-Haloalkoxide (n-Bu3SnO(CH2)nX) with Isothiocyanate
Baba, Akio,Shibata, Ikuya,Kashiwagi, Hiroki,Matsuda, Haruo
, p. 341 - 343 (2007/10/02)
Tri-n-butyltin ω-haloalkoxides are useful reagents for the preparation of sulfur-containing five- and six-membered cyclic compounds combined with isothiocyanates.
