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- Hydrophilic phase transfer catalyst based on the sulfoacid group and polyoxometalate for the selective oxidation of sulfides in water with hydrogen peroxide. Wei Zhao, Chunxia Yang, Kecheng Liu, Ying Yang, Tao Chang
, New J. Chem.
, 2017
, 41
, 447
- A reusable catalytic system for sulfide oxidation and epoxidation of allylic alcohols in water catalyzed by poly(dimethyl diallyl) ammonium/polyoxometalate. Wei Zhao, Chunxia Yang, Zhiguo Cheng, Zhenghui Zhang
, Green Chem.
, 2016
, 18
, 995
- CXL.—Accelerated formation of magnesium alkyl and aryl haloids. Harry Hepworth
, J. Chem. Soc., Trans.
, 1921
, 119
, 1249
- CCCVI.—Influence of poles and polar linkings on the course pursued by elimination reactions. Part IV. Further experiments on the olefinic degradation of sulphones. Geoffrey William Fenton, Christopher Kelk Ingold
, J. Chem. Soc.
, 1929
, 2338
- 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
- Branched-chain thia-alkanebis(quaternary ammonium) salis as ganglion-blocking agents. K. J. M. Anerews, F. Bergel, A. L. Morrison
, J. Chem. Soc.
, 1954
, 3483
- 595. Thia- and dithia-alkanebis(quaternary ammonium) salts as neuromuscular- and ganglion-blocking agents. K. J. M. Andrews, F. Bergel, A. L. Morrison
, J. Chem. Soc.
, 1953
, 2998
- Novel SN2 ring-opening reactions of 2- and 2,2-substituted thiiranes with thiols using Na+-exchanged X-type zeolite or triethylamine in methanol. Hiroshi Takeuchi, Yasuhisa Nakajima
, J. Chem. Soc., Perkin Trans. 2
, 1998
, 2441
- Green catalysis for the selective oxidation of sulfides with high turnover numbers in water at room temperature. Wei Zhao, Chunxia Yang, Hongxian Sun, Zhiguo Cheng, Tao Chang
, New J. Chem.
, 2018
, 42
, 19349
- CXCI.—The relation between residual affinity and chemical constitution. Part III. Some heterocyclic compounds. Hans Thacher Clarke
, J. Chem. Soc., Trans.
, 1912
, 101
, 1788