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Reaction Involving (reaction + involving)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

Brønsted Acid Catalyzed Enantioselective Three-Component Reaction Involving the ,,Addition of Isocyanides to Imines,

ANGEWANDTE CHEMIE, Issue 36 2009
Tao Yue
Traute Dreisamkeit: Dreikomponentenreaktionen von Aldehyden, Anilinen und ,-Isocyanacetamiden in Gegenwart eines chiralen Phosphorsäurederivats als Katalysator ergeben die 5-(1-Aminoalkyl)-5-aminooxazole 1 in ausgezeichneten Ausbeuten und mit mittleren bis guten Enantiomerenüberschüssen (siehe Schema). [source]

ChemInform Abstract: Water-Controlled Regioselectivity of Pd-Catalyzed Domino Reaction Involving a C,H Activation Process: Rapid Synthesis of Diverse Carbo- and Heterocyclic Skeletons.

CHEMINFORM, Issue 26 2010
Zhiyao Lu
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 5-Methylindole-4,7-quinone Through a New Construction of the Functionalized Indole Ring Based on the Allene-Mediated Electrocyclic Reaction Involving the Pyrrole[b]-Bond.

CHEMINFORM, Issue 50 2004
Maho Hirayama
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

A novel three-component one-pot reaction involving ,-naphthol, aldehydes, and urea promoted by TMSCl/NaI

JOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 2 2010
Gowravaram Sabitha
Amidoalkyl naphthol derivatives have been synthesized in good yields in a one-pot condensation of ,-naphthol, aromatic aldehydes and urea in presence of TMSCl/NaI at room temperature. Ring closure of amidoalkyl naphthol derivatives occurred at 140°C to afford 1,2-dihydro-1-arylnaphtho[1,2-e] [1,3]oxazin-3-one derivatives. J. Heterocyclic Chem., (2010). [source]

ChemInform Abstract: Gold-Catalyzed Domino Reactions Consisting of Regio- and Stereoselective 1,2-Alkyl Migration.

CHEMINFORM, Issue 43 2010
Wenbo Li
Abstract A cationic gold(I)-catalyzed domino reaction involving highly regio- and stereoselective 1,2-alkyl migration and heterocyclization or oxygen transfer is developed, in which the product selectivity is controlled by the counteranion of the gold catalyst. [source]