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Vinyl Arenes (vinyl + arene)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: Catalytic Asymmetric Synthesis Using Feedstocks: An Enantioselective Route to 2-Arylpropionic Acids and 1-Arylethyl Amines via Hydrovinylation of Vinyl Arenes

CHEMINFORM, Issue 35 2009
Craig R. Smith
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: InX3 -Catalyzed Haloamidation of Vinyl Arenes: A Facile Synthesis of ,-Bromo- and ,-Fluoroamides.

CHEMINFORM, Issue 25 2009
J. S. Yadav
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]

Bismuth- and Hafnium-Catalyzed Hydroamination of Vinyl Arenes with Sulfonamides, Carbamates, and Carboxamides.

CHEMINFORM, Issue 17 2007
Hongbo Qin
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, please click on HTML or PDF. [source]

Bismuth- and Hafnium-Catalyzed Hydroamination of Vinyl Arenes with Sulfonamides, Carbamates, and Carboxamides

CHEMISTRY - AN ASIAN JOURNAL, Issue 1 2007
Hongbo Qin
Abstract Catalytic intermolecular hydroamination of vinyl arenes is described. Our initial investigation revealed that a Bi(OTf)3/[Cu(CH3CN)4]PF6 system previously developed for catalytic intermolecular hydroamination of 1,3-dienes was suitable for hydroamination of a styrene with sulfonamides, but the substrate generality of this system was unsatisfactory. Several metals were screened to expand the substrate scope, and a new Hf(OTf)4/[Cu(CH3CN)4]PF6 system was determined to be highly suitable. The combination of Hf(OTf)4 and [Cu(CH3CN)4]PF6 efficiently promoted the hydroamination of various vinyl arenes, including less-reactive vinyl arenes with electron-withdrawing groups. This strategy was applied to sulfonamides, carbamates, and carboxamides, and products were obtained in up to 99,% yield with 0.3,10,mol,% catalyst loading. [source]