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Oxidative Coupling Reactions (oxidative + coupling_reaction)

Distribution by Scientific Domains

Chemistry	80%

Selected Abstracts

ChemInform Abstract: Diversity-Oriented Synthesis of Benzimidazole, Benzoxazole, Benzothiazole and Quinazolin-4(3H)-one Libraries via Potassium Persulfate,CuSO4 -Mediated Oxidative Coupling Reactions of Aldehydes in Aqueous Micelles.

CHEMINFORM, Issue 37 2010
Atul Kumar
Abstract The diversity-oriented synthesis of the title heterocycles in aqueous micelles shows the advantages of short reaction times, high yields, high chemoselectivities, low coast, and environmental friendliness. [source]

ChemInform Abstract: Nickel-Catalyzed Oxidative Coupling Reactions of Two Different Terminal Alkynes Using O2 as the Oxidant at Room Temperature: Facile Syntheses of Unsymmetric 1,3-Diynes.

CHEMINFORM, Issue 25 2009
Weiyan Yin
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

ChemInform Abstract: VO(acac)2 -Catalyzed Oxidative Coupling Reactions of Phosphonium Salts.

CHEMINFORM, Issue 27 2002
Min Shi
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Synthesis of a Novel Oligoaniline: "Dumbbell-Shaped" Oligoaniline,

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 5 2004
Youhai Yu
Abstract Summary: A new kind of aniline oligomer with a "dumbbell" shape was synthesized through a simple oxidative coupling reaction with a new rigid aromatic amine as starting material. The oligomer was characterized with mass spectrometry, IR and NMR spectroscopies. Its redox property was checked by cyclic voltammetry and chemical oxidation/reduction process was monitored by UV spectroscopy. We found it has a reversible electrochemical property like common oligoanilines. Combined with its well-defined structure, it is expected to act as a model compound for a molecular electronic switch. The "dumbbell-shaped" oligoaniline compound synthesized here. [source]

Synthesis of (-)-herbertenediol and (aR, aS)-mastigophorenes A via asymmetric intramolecular heck coupling reaction,

CHINESE JOURNAL OF CHEMISTRY, Issue 12 2001
Ai-Min Zhang
Abstract Total enantioselective synthesis of the natural (-)-Herbertenediol (1) was accomplished in eleven steps with an overall yield of 15% starting from the 2-methoxy-4-methyl-phenol. The total synthesis features asymmetric intramolecular Heck reaction and Wolff-Kishner-Huang reduction. (aR, aS)-Mastigophorenes A was also synthesized through the oxidative coupling reaction. [source]