Results
1 -
10 of
61
(Click
here to explore results)
- Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide. Caleb A. Class, Mengjie Liu, Aäron G. Vandeputte, William H. Green
, Phys. Chem. Chem. Phys.
, 2016
, 18
, 21651
- Photosensitized oxidation of phenyl and tert-butyl sulfides. Sergio M. Bonesi, Maurizio Fagnoni, Sandra Monti, Angelo Albini
, Photochem. Photobiol. Sci.
, 2004
, 3
, 489
- Magneli-type tungsten oxide nanorods as catalysts for the selective oxidation of organic sulfides. René Dören, Jens Hartmann, Benjamin Leibauer, Martin Panthöfer, Mihail Mondeshki, Wolfgang Tremel
, Dalton Trans.
, 2021
, 50
, 14027
- Use of a neural network to determine the normal boiling points of acyclic ethers, peroxides, acetals and their sulfur analogues. Driss Cherqaoui, Didier Villemin, Abdelhalim Mesbah, Jean-Michel Cense, Vladimir Kvasnicka
, J. Chem. Soc., Faraday Trans.
, 1994
, 90
, 2015
- Ultra-mild synthesis of nanometric metal chalcogenides using organyl chalcogenide precursors. Shashank Mishra
, Chem. Commun.
, 2022
, 58
, 10136
- Index of subjects, 1947
, J. Chem. Soc.
, 1947
, 1720
- Vapor phase catalytic photooxidation of sulfides to sulfoxides: application to the neutralization of sulfur mustard simulants. Emmanuel Oheix, Edmond Gravel, Eric Doris
, Catal. Sci. Technol.
, 2022
, 12
, 1751
- A kinetic investigation, supported by theoretical calculations, of steric and ring strain effects on the oxidation of sulfides and sulfoxides by dimethyldioxirane in acetone. Peter Hanson, Ramon A. A. J. Hendrickx, John R. Lindsay Smith
, New J. Chem.
, 2010
, 34
, 65
- Alkylaluminum dichloride–ether complexes which are fully soluble in hydrocarbons as catalysts for the synthesis of exo-olefin terminated polyisobutylene at room temperature. Irina V. Vasilenko, Dmitriy I. Shiman, Sergei V. Kostjuk
, Polym. Chem.
, 2014
, 5
, 3855
- 299. The reaction of sulphur and sulphur compounds with olefinic substances. Part II. Mechanism of the reaction of hydrogen sulphide with mono-olefins, di-isoprenes, and rubber. Ralph F. Naylor
, J. Chem. Soc.
, 1947
, 1532