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I2/PhI(OAc)2 Copromoted Amination Reaction: Synthesis of α-Dicarbonylsulfoximine Derivatives by Incorporating an Intact Dimethyl Sulfoxide.

Journal of Organic Chemistry, 2019
An I2/PhI(OAc)2 copromoted strategy using dimethyl sulfoxide as an "S/C2/O" source for preparing α-dicarbonylsulfoximine derivatives is reported. This process involves oxidative coupling to construct a C-N bond and electrophilic amination of dimethyl ...
Peng Zhao   +6 more
semanticscholar   +1 more source

Quantifying Hydrogen-Bond Populations in Dimethyl Sulfoxide/Water Mixtures.

Angewandte Chemie, 2017
Dimethyl sulfoxide (DMSO) disrupts the hydrogen-bond networks in water. The widespread use of DMSO as a cosolvent, along with its unusual attributes, have inspired numerous studies.
Kwang-Im Oh   +3 more
semanticscholar   +1 more source

Thermolysis of dimethyl sulfoxide

International Journal of Chemical Kinetics, 1973
AbstractThe thermal decomposition of dimethyl sulfoxide at small extent of reaction has been studied at temperatures of 297‐350°C and pressures of 10–400 Torr. The major products CH4, C2H4, and SO2 were shown to follow first‐order kinetics. The activation energies for production of each was about 48 kcal·mole−1. A chain mechanism has been postulated in
G. Debecker, F. C. Thyrion
openaire   +3 more sources

DIMETHYL SULFOXIDE THERAPY IN BRONCHIOLITIS

Annals of the New York Academy of Sciences, 1975
The action of a medicinal spray that contains anti-inflammatory and bacterio-static drugs integrated with the penetrating and potentiating agent DMSO has been evaluated clinically in 60 infants with acute respiratory obstruction. A dose of 2 ml of this spray is applied in the posterior pharynx and the tonsil region; 1 to 4 applications are made ...
Rodolfo Burdach   +2 more
openaire   +3 more sources

Dimethyl Sulfoxide Involved One-Pot Synthesis of Quinoxaline Derivatives.

Journal of Organic Chemistry, 2017
An efficient, green, and novel method for the synthesis of N-heterocycle-fused quinoxalines is reported herein. Dimethyl sulfoxide was used as both a reactant and a solvent in this reaction.
Caixia Xie   +6 more
semanticscholar   +1 more source

Transition Metal-Free α-Csp3-H Methylenation of Ketones to Form C═C Bond Using Dimethyl Sulfoxide as Carbon Source.

Journal of Organic Chemistry, 2017
A direct α-Csp3-H methylenation of arylketones to form C═C bond using dimethyl sulfoxide as one-carbon source is achieved under transition metal-free reaction condition.
Yufeng Liu   +6 more
semanticscholar   +1 more source

Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: Sulfenylation of Enaminones Using Dimethyl Sulfoxide as an Oxidant.

Journal of Organic Chemistry, 2017
Synthesis of polyfunctionalized aminothioalkenes has been demonstrated using iodine as a catalyst (30 mol %) and dimethyl sulfoxide as an oxidant under metal-free reaction conditions.
Yogesh Siddaraju, K. R. Prabhu
semanticscholar   +1 more source

Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: A Regioselective Sulfenylation of Imidazoheterocycles Using Dimethyl Sulfoxide as an Oxidant.

Journal of Organic Chemistry, 2016
A regioselective formation of C-S bonds has been achieved using a cross dehydrogenative coupling (CDC) protocol using iodine as a catalyst and dimethyl sulfoxide as an oxidant under green chemistry conditions. This strategy employs the reaction of easily
Yogesh Siddaraju, K. R. Prabhu
semanticscholar   +1 more source

Dimethyl Sulfide and Dimethyl Sulfoxide and Their Oxidation in the Atmosphere

Chemical Reviews, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Nikos Mihalopoulos   +2 more
openaire   +4 more sources

DIMETHYL SULFOXIDE

1961
Although dimethyl sulfoxide was first synthesized in 1866, it remained a curiosity for many years. Recently, however, the group of lower aliphatic sulfoxides has been the object of increased attention. Availability of cheap dimethyl sulfide from the “black liquor” of sulfite pulp manufacture prompted research which led to the development of ...
William O. Ranky, Douglas C. Nelson
openaire   +2 more sources

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