82843-64-9Relevant academic research and scientific papers
Triethylamine-catalyzed one-pot synthesis of trithiocarbonates from carbon disulfide, thiols, and alkyl halides in water
Movassagh, Barahman,Soleiman-Beigi, Mohammad
experimental part, p. 927 - 930 (2009/09/06)
Symmetrical and unsymmetrical trithiocarbonates were prepared by a simple and efficient one-pot reaction of thiols, carbon disulfide, and alkyl halides in the presence of triethylamine in water at room temperature.
Zinc thiolate complexes [ZnLn(SR)]+ with azamacrocyclic ligands, part II: Mechanism of the reaction with CS2
Notni, Johannes,Schenk, Stephan,Roth, Arne,Plass, Winfried,Goerls, Helmar,Uhlemann, Ute,Walter, Angela,Schmitt, Michael,Popp, Juergen,Chatzipapadopoulos, Susana,Emmler, Thomas,Breitzke, Hergen,Leppert, Joerg,Buntkowsky, Gerd,Kempe, Kristian,Anders, Ernst
, p. 2783 - 2791 (2007/10/03)
The thiolate complexes [Zn([15]aneN4)(S-CH2-C 6H5)]ClO4 (1) ([15]aneN4 = 1,4,8,12-tetraazacyclopentadecane) and [Zn(i-[14]aneN4)(S-CH 2-C6H5)]ClO
Synthesis and Lithiation of 2-Alkylthio- and 2-Arylthio-1,3-dithiolanes
Tanimoto, Shigeo,Oida, Tatsuo,Ikehira, Hideyuki,Okano, Masaya
, p. 1977 - 1978 (2007/10/02)
Several 2-alkylthio- and 2-arylthio-1,3-dithiolanes were synthesized by the reaction of 2-ethoxy-1,3-dithiolane with aliphatic and aromatic thiols in the presence of ZnCl2.The lithiation of 2-alkylthio-1,3-dithiolanes with butyllithium in tetrahydrofuran followed by the addition of alkyl halides gave unsymmetrical dialkyl trithiocarbonates in moderately good yields.
