| 1 |
Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent
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ORGANIC & BIOMOLECULAR CHEMISTRY
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| 2 |
NiFe2O4 as a magnetically recoverable nanocatalyst for odourless C–S bond formation via the cleavage of C–O bond in the presence of S8 under mild and green conditions
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APPLIED ORGANOMETALLIC CHEMISTRY
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| 3 |
Co(II)-catalyzed regioselective clean and smooth synthesis of 2-(aryl/alkylthio) phenols via sp2 C-H bond activation
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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
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| 4 |
Laccase-catalyzed, aerobic oxidative coupling of 4-substituted urazoles with sodium arylsulfinates: Green and mild procedure for the synthesis of arylsulfonyl triazolidinediones
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TETRAHEDRON LETTERS
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| 5 |
Efficient Cu-catalyzed one-pot odorless synthesis of sulfides from triphenyltin chloride, aryl halides and S8 in PEG
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TETRAHEDRON LETTERS
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| 6 |
Ligand-free Cu-catalyzed odorless synthesis of unsymmetrical sulfides through cross-coupling reaction of aryl/benzyl/alkyl halides with an aryl boronic acid/S8 system as a thiolating agent in PEG
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RSC advances
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| 7 |
Trichloroisocyanuric acid (TCCA) as a mild and efficient catalyst for the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) under heterogonous conditions
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CATALYSIS COMMUNICATIONS
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| 8 |
Microwave-Assisted Chemoselective Regeneration of Carbonyl Compounds from Oximes by Silica Chromate/WET SiO2 under Solvent-Free Conditions
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Phosphorus Sulfur and Silicon
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| 9 |
Acylation of alcohols catalyzed by using 1,3-dibromo-5,5-dimethylhydentoin or trichloroisocyanuric acid
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CATALYSIS COMMUNICATIONS
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| 10 |
1,3-Dichloro-5,5-dimethylhydantoin (DCH) and Trichloromelamine (TCM) as Efficient Catalysts for the Chemoselective Trimethylsilylation of Hydroxyl Group with 1,1,1,3,3,3-Hexamethyldisilazane (HMDS) under Mild Conditions
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Journal of the Chinese Chemical Society
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| 11 |
Ferric nitrate in the presence of catalytic amounts of KBr and/or NaBr: an efficient and homoselective catalytic media for the selective oxidation of sulfides to sulfoxides
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MONATSHEFTE FUR CHEMIE
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| 12 |
Selective and Efficient Oxidation of Sulfides to Sulfoxides Using Ammonium Cerium (IV) Nitrate (CAN) in the presence of a catalytic amount of KBr or NaBr
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MONATSHEFTE FUR CHEMIE
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| 13 |
Chemo and homoselective catalytic oxidation of sulfides to sulfoxides with supported nitric acid on silica gel and poly vinyl pyrrolidone (PVP) catalyzed by KBr and/or NaBr
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CATALYSIS COMMUNICATIONS
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