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Highly Enantio (highly + enantio)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: Highly Enantio- and Diastereoselective Michael Addition of Cyclohexanone to Nitroolefins Catalyzed by a Chiral Glucose-Based Bifunctional Secondary Amine,Thiourea Catalyst.

CHEMINFORM, Issue 51 2009
Aidang Lu
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: Highly Enantio- and Diastereoselective Organocatalytic Cascade Aza-Michael,Michael Reactions: A Direct Method for the Synthesis of Trisubstituted Chiral Pyrrolidines.

CHEMINFORM, Issue 14 2009
Hao Li
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]

A Highly Enantio- and Diastereoselective 1,3-Dimethylallylation of Aldehydes.

CHEMINFORM, Issue 10 2007
Yu Yuan
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]

A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter Reaction.

CHEMINFORM, Issue 38 2005
Javier Read de Alaniz
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

The Enantioselective, Organocatalyzed Diels,Alder Reaction of 2-Vinylindoles with ,,,-Unsaturated Aldehydes: An Efficient Route to Functionalized Tetrahydrocarbazoles

CHEMISTRY - A EUROPEAN JOURNAL, Issue 20 2010
Changwu Zheng Dr.
Prolinol catalysts: A highly enantio- and diastereoselective prolinol-catalyzed Diels,Alder reaction of 2-vinylindoles and ,,,-unsaturated aldehydes is developed (see scheme). This methodology allows the development of further applications of prolinols in asymmetric synthesis. The resulting densely functionalized enantiomerically pure tetrahydrocarbazoles are useful in the total synthesis of natural products such as the core structure of the akuammiline alkaloid vincorine. [source]