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Nitroaldol Reaction (nitroaldol + reaction)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: Chiral Binuclear Copper(II) Catalyzed Nitroaldol Reaction: Scope and Mechanism.

CHEMINFORM, Issue 19 2009
Suribabu Jammi
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]

Zinc,Proline Complex: An Efficient, Reusable Catalyst for Direct Nitroaldol Reaction in Aqueous Media.

CHEMINFORM, Issue 45 2007
K. Rajender Reddy
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]

Enantioselective Nitroaldol Reaction of ,-Ketoesters Catalyzed by Cinchona Alkaloids.

CHEMINFORM, Issue 23 2006
Hongming 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, please click on HTML or PDF. [source]

Synthesis, Structure, and Application of Self-Assembled Copper(II) Aqua Complex by H-Bonding for Acceleration of the Nitroaldol Reaction on Water

CHEMISTRY - AN ASIAN JOURNAL, Issue 2 2009
Suribabu Jammi
Abstract Simple addition: Copper(II) aqua complex 1 can be prepared in a one-pot synthesis and is self-assembled by H-bond interactions. Complex 1 is shown to accelerate the nitroaldol reaction on water, which is a heterogeneous process, requiring no additive or base, and 1 can be recycled without loss of activity. Copper(II) aqua complex 1 has been prepared in a one-pot synthesis. The single crystal X-ray analysis showed that the complex is self-assembled through aqua ligands by H-bond interactions and the copper(II) atoms are pentacoordinated with square pyramidal geometry. Complex 1 has been studied for the acceleration of the nitroalodol reaction on water. It is a clean technological process and the catalyst can be recycled without loss of activity. [source]