145 research outputs found
Palladium NanoparticlesImmobilized on Nano-silica Triazine Dendritic Polymer (Pdnp-nSTDP): An Efficient and Reusable Catalyst for Suzuki-Miyaura Cross-Coupling and Heck Reactions
A new catalyst based on palladium nanoparticles immobilized on nano-silica triazine dendritic polymer (Pdnp-nSTDP) was synthesized and characterized by FT-IR spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, energy dispersive X-ray, transmission electron microscopy and elemental analysis. The size of the palladium nanoparticles was determined to be 3.1±0.5 nm. This catalytic system showed high activity in the Suzuki–Miyaura cross-coupling of aryl iodides, bromides and chlorides with arylboronic acids and also in the Heck reaction of these aryl halides with styrenes. These reactions were best performed in a dimethylformamide (DMF)/water mixture (1:3) in the presence of only 0.006 mol% and 0.01 mol% of the catalyst, respectively, under conventional conditions and microwave irradiation to afford the desired coupling products in high yields. The Pdnp-nSTDP was also used as an efficient catalyst for the preparation of a series of star- and banana-shaped compounds with a benzene, pyridine, pyrimidine or 1,3,5-triazine unit as the central core. Moreover, the catalyst could be recovered easily and reused several times without any considerable loss of its catalytic activity
Selective Oxidative Cleavage of Benzylic and Allylic Oximes to Their Carbonyl Compounds with Strontium Manganate in the Presence of Aluminum Chloride in Solution and under Solvent‐Free Conditions.
Efficient and selective deprotection of aryl aldehyde diacetates catalyzed by tin(II) chloride dihydrate
1223-1225A mild,efficient
and excellent yield method for the selective deprotection of
aryl aldehyde diacetates in the presence
of .phenolic acetate and aliphatic aldehyde diacetate using catalytic
amounts of tin(II) chloride dihydrate (SnCl2.2H2O) is
described
ChemInform Abstract: 3-Carboxypyridinium Chlorochromate: An Inexpensive and Efficient Reagent for Cleavage of Carbon-Nitrogen Double Bonds under Non-Aqueous Condition.
ChemInform Abstract: Bi(III) Salts as New Catalysts for the Selective Conversion of Trimethylsilyl and Tetrahydropyranyl Ethers to Their Corresponding Acetates and Formates.
Antimony trichloride; a mild, efficient and convenient catalyst for conversion of oxiranes to thiiranes under non-aqueous conditions
605-606<span style="font-size:12.0pt;font-family:
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-in;mso-fareast-language:en-in;mso-bidi-language:ar-sa"="" lang="EN-IN">Oxiranes are
converted to their corresponding thiiranes in excellent yields (95-98%) using
ammoniun thiocyailate and catalytic amounts of antimony trichloride.</span
Silica Chloride–Catalyzed Synthesis of Thiiranes from Oxiranes Under Solvent-Free Conditions
ChemInform Abstract: Antimony Trichloride: A Mild, Efficient, and Convenient Catalyst for Conversion of Oxiranes to Thiiranes under Non-Aqueous Conditions.
Selective Oxidation of Benzylic and Allylic Alcohols Using Strontium Manganate in the Presence of Lewis Acids in Solution and under Solvent‐Free Conditions.
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