Copper(II) complexes of two TEMPO-functionalized polypyridyl ligands: structure and catalytic activity in alcohol oxidation.
The preparation of carboxylic acids can be accomplished by the oxidation of a number of functional groups using a wide variety of reagents. Mark C. Noe,, Joel M. Hawkins,, Sheri L. Snow, and.
N Recent Strategies in Preparation of Cellulose Nanocrystals and Cellulose Nanofibrils Derived from Raw Cellulose Materials. The carboxyl group (COOH) gets its name because of the carbonyl group (C=O) and a hydroxyl group. Synthesis of carboxylic acids by oxidation of benzylic substrates. Carboxylic acid is an organic compound in which a carbon atom is doubly bonded to an oxygen atom and with a hydrogen atom with a single bond. Here we report that single Rh atom sites, Rh1O5 anchored in micropores of HZSM-5, can catalyze oxidation of ethane by hydrogen peroxide in aqueous solution to form acetic acid and formic acid at a temperature ≤ 50 °C at a pressure of ethane at 1.5 bar. Yun Ma, Colin Loyns, Peter Price, Victor Chechik. As an intermediate product, aldehyde is given. Your Mendeley pairing has expired. Review: Catalytic oxidation of cellulose with nitroxyl radicals under aqueous conditions. Hirofumi Tohma, Shinobu Takizawa, Tomohiro Maegawa, Yasuyuki Kita. A REVIEW. Masatoshi Shibuya, Takahisa Sato, Masaki Tomizawa, Yoshiharu Iwabuchi.
Kinga Kędziora, Alba Díaz-Rodríguez, Iván Lavandera, Vicente Gotor-Fernández, Vicente Gotor. Mathias Ibert, Francis Marsais, Nabyl Merbouh, Christian Brückner. Adsorption of poly(3-octylthiophene) nanoparticles on cellulose fibres: Effect of dispersion stability and fibre pre-treatment with carboxymethyl cellulose. Preparation of oxidized celluloses in a TEMPO/NaBr system using different chlorine reagents in water. Cr (VI) reagents are the most common used oxidation reagents. Zhiguo J. Song,, Mangzhu Zhao,, Richard Desmond,, Paul Devine,, David M. Tschaen,, Richard Tillyer,, Lisa Frey,, Richard Heid,, Feng Xu,, Bruce Foster,, Jing Li,, Robert Reamer,, Ralph Volante,, Edward J. J.Grabowski,, Ulf H. Dolling, and, Paul J. Reider, , Shigemitsu Okada,, Yoshiaki Kato, and. Alexander Barthel, Sebastian Stark, René Csuk. Colloids and Surfaces A: Physicochemical and Engineering Aspects. via Total syntheses of spiroviolene and spirograterpene A: a structural reassignment with biosynthetic implications. TEMPO/HCl/NaNO2 Catalyst: A Transition-Metal-Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions. TEMPO Electromediated Oxidation of Some Polysaccharides Including Regenerated Cellulose Fiber. Novel Synthesis of Carbamate-Linked Oligosaccharides by a Modified Curtius Rearrangement. in situ dihydrido carbonyl PNP complexes. Remarkably chemoselective indium-mediated coupling en route to the C21–C40 acyclic portion of the azaspiracids. Akira Isogai, Tuomas Hänninen, Shuji Fujisawa, Tsuguyuki Saito. F.Javier Moreno-Dorado, Francisco M. Guerra, Marı́a J. Ortega, Eva Zubı́a, Guillermo M. Massanet. Efficient Total Synthesis of Bongkrekic Acid and Apoptosis Inhibitory Activity of Its Analogues.
Find more information about Crossref citation counts. Clean and Highly Selective Oxidation of Alcohols in an Ionic Liquid by Using an Ion-Supported Hypervalent Iodine(III) Reagent. Hironori Tsunoyama, Tatsuya Tsukuda, Hidehiro Sakurai. 400 nm blue light-emitting diode.
The oxidation of primary alcohols to carboxylic acids is an important oxidation reaction in organic chemistry. Synthetic Studies of 2,2-Difluorobicyclo[1.1.1]pentanes (BCP-F syn trans The oxonium ion loses a proton to the nitrogen atom, forming an enol. Organic Process Research & Development 2017 , 21 (9) , 1388-1393. Fe Spin Trapping of Au−H Intermediate in the Alcohol Oxidation by Supported and Unsupported Gold Catalysts. Total Synthesis and Initial Biological Evaluation of New B-Ring-Modified Bryostatin Analogs. PREPARATION OF TETRAMETHYLPIPERDINE-1-OXOAMMONlUM SALTS AND THEIR USE AS OXIDANTS IN ORGANIC CHEMISTRY. 2 Zhenhua Dong, Pengwei Gao, Yongmei Xiao.
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