Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions.

Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Research Abstract Details 

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Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Abstract Text:

Liansuo Zu,Hao Li,Hexin Xie,Jian Wang,Wei Jiang,Yun Tang,Wei Wang,

Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Publishing Authors By Initials

L Zu,H Li,H Xie,J Wang,W Jiang,Y Tang,W Wang,

For similar natural sciences: chemistry: chemistry, organic: isomerism: stereoisomerism research abstracts see: natural sciences: chemistry: chemistry, organic: isomerism: stereoisomerism research

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Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Journal Published:

PUBLICATION TYPE: Research Support, Non-U.S. Gov

Journal: Angewandte Chemie (International ed. in English)

VOLUME: 46

Page Numbers: 3732-4

Journal Abbreviation: Angew. Chem. Int. Ed. Engl.

ISSN: 1433-7851

DAY: 3

MONTH: 12

YEAR: 2007

Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Information

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LANGUAGE: eng

NlmUniqueID: 370543

Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Keywords Mesh Terms:

KEYWORDS: Stereoisomerism

MESH TERMS: chemistry

Chemical & Substance for Abstract: Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Information

Substance Name: Cyclopentanes

Registry Number: 0

Grant and Affiliation Information for Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions.

AFFILIATION: Department of Chemistry, University of New Mexico, MSC03 2060, Albuquerque, NM 87131-0001, USA.

Country: Germany

AGENCY: United States NCRR

GRANT: P20 RR16480

ACRONYM: RR

MEDLINETA: Angew Chem Int Ed Engl

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