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Amines Catalyzed (amine + catalyze)

Distribution by Scientific Domains
Chemistry100%
Distribution within Chemistry
Organic Chemistry80%
General & Introductory Chemistry20%

Selected Abstracts

Microwave-Promoted, Solvent-Free, Three-Component Coupling of Aldehyde, Alkyne, and Amine Catalyzed by AgNO3.

CHEMINFORM, Issue 32 2007
Tingting He
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]

Oxidative Amidation of Aldehydes and Alcohols with Primary Amines Catalyzed by KI-TBHP

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 21 2008
K. Rajender Reddy
Abstract Oxidative amidation of aldehydes and alcohols with amines to afford the corresponding amides in excellent yields and ee values over 98,% is achieved by using a catalytic amount of KI in combination with TBHP as the external oxidant. This method avoids the use of expensive and/or air-sensitive reagents. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

ChemInform Abstract: Synthesis of Urea Derivatives from CO2 and Amines Catalyzed by Polyethylene Glycol Supported Potassium Hydroxide Without Dehydrating Agents.

CHEMINFORM, Issue 36 2010
De-Lin Kong
Abstract A simple catalyst is developed and efficiently used for the fixation of carbon dioxide as symmetrical urea derivatives. [source]

ChemInform Abstract: Efficient Synthesis of ,-Oxoalkyl Carbamates from Carbon Dioxide, Internal Propargylic Alcohols, and Secondary Amines Catalyzed by Silver Salts and DBU.

CHEMINFORM, Issue 35 2010
Chaorong Qi
Abstract The cooperation between AgOAc and DBU is a key factor in activating the transformation. [source]

ChemInform Abstract: Highly Efficient Michael Addition Reaction of Amines Catalyzed by Silica-Supported Aluminum Chloride.

CHEMINFORM, Issue 33 2009
Mohammad R. Saidi
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]

Enantioselective Ring Opening of meso-Epoxides by Aromatic Amines Catalyzed by Lanthanoid Iodo Binaphtholates.

CHEMINFORM, Issue 32 2005
Fabien Carree
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

An Efficient Method for the Ring Opening of Epoxides with Aromatic Amines Catalyzed by Bismuth Trichloride.

CHEMINFORM, Issue 3 2003
Thierry Ollevier
No abstract is available for this article. [source]

ChemInform Abstract: An Efficient Method for the Ring Opening of Epoxides with Aromatic Amines Catalyzed by Indium Trichloride.

CHEMINFORM, Issue 24 2001
L. Rajender Reddy
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]

Direct Dehydrogenative Amide Synthesis from Alcohols and Amines Catalyzed by ,-Alumina Supported Silver Cluster

CHEMISTRY - A EUROPEAN JOURNAL, Issue 39 2009
Ken-ichi Shimizu Dr.
Silver clusters immobilized on ,-Al2O3 catalyze direct amide synthesis from alcohols and amines in the presence of catalytic amount of weak base (Cs2CO3). The reaction proceeds by cooperation of the coordinatively unsaturated silver site, as well as acid and base sites of the oxide support (see scheme). [source]

Three-component Synthesis of Homoallylic Amines Catalyzed by Phosphomolybdic Acid in Water

CHINESE JOURNAL OF CHEMISTRY, Issue 5 2009
Zhengfeng XIE
Abstract The three-component reactions of aromatic aldehydes, amines and allyltributylstannane in water catalyzed by phosphomolybdic acid (PMA), underwent smoothly to afford the corresponding homoallylic amines in high yields at room temperature. [source]