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Synthesis, Structures, Electrochemistry, and Catalytic Activity towards Cyclohexanol Oxidation of Mono-, Di-, and Polynuclear Iron(III) Complexes with 3-Amino-2-Pyrazinecarboxylate-O)[1/2](Na)(μ-H[2]O)[1/2]]n(4), are reported. Reactions of 3-amino-2-pyrazinecarboxylic acid (HL

Synthesis, Structures, Electrochemistry, and Catalytic Activity towards Cyclohexanol Oxidation of Mono-, Di-, and Polynuclear Iron(III) Complexes with 3-Amino-2-Pyrazinecarboxylate), are reported. Reactions of 3-amino-2-pyrazinecarboxylic acid (HL) with iron(III) chloride under di erent

Chapter 4: The Vanadate-Pyrazinecarboxylic Acid-Hydrogen Peroxide Reagent and Similar Systems for Efficient Oxidations with PeroxidesA simple vanadate anion VO3- does not catalyse various oxidations with hydrogen peroxide via

Disordered residues and patterns in the protein data bank, patterns consisting of two kinds of amino acids, and homo-repeats. Using this database, the user can: (1

Rh(III)-Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with CF3-Containing α-Propargyl α-Amino Acid DerivativesA series of new orthogonally protected α-CF3-substituted α-amino carboxylates, and α-amino

Rh(III)-Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with CF3-Containing α-Propargyl α-Amino Acid DerivativesA series of new orthogonally protected α-CF3-substituted α-amino carboxylates, and α-amino

3-Amino-1,2,4-triazolium salts as NHC-proligands: synthesis and postmodification of a new type of amino-functionalized Pd/NHC complexes were obtained by direct palladation of 3-amino-1,4-dialkyl-1,2,4-triazolium salts. These amino

Synthesis of water-soluble amino functionalized multithiacalix[4]arene via quaternization of tertiary amino groups
containing amino groups and phthalimide fragments by the formation of quaternary ammonium salts is presented

Mixed-ligand platinum(IV) complexes with amino acids and cytosine < His. Reactions of aqueous solutions yields the following complexes: Pt(Cyt)(Gly-)Cl33H2O (I

Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compounds converted into 1,7-diaryl-3-amino-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-ones and 3-(2-amino-4-aryl-1H

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