Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline.

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Research Abstract Details 

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Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Abstract Text:

Barry M Trost,Megan K Brennan,

[reaction; see text] The asymmetric synthesis of the oxindole alkaloid horsfiline is described. A palladium-catalyzed asymmetric allylic alkylation (AAA) is used to set the spiro(pyrrolidine-oxindole) stereogenic center.

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Publishing Authors By Initials

BM Trost,MK Brennan,

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

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MEDLINE DATE:

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Journal Published:

PUBLICATION TYPE: Research Support, U.S. Gov't,

Journal: Organic letters

VOLUME: 8

Page Numbers: 2027-30

Journal Abbreviation: Org. Lett.

ISSN: 1523-7060

DAY: 11

MONTH: May

YEAR: 2006

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 100890393

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Keywords Mesh Terms:

KEYWORDS: Stereoisomerism

MESH TERMS: chemistry

Chemical & Substance for Abstract: Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Information

Substance Name: Palladium

Registry Number: 7440-05-3

Grant and Affiliation Information for Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline.

AFFILIATION: Department of Chemistry, Stanford University, California 94305, USA. bmtrost@stanford.edu

Country: United States

AGENCY: United States NIGMS

GRANT: GM33049

ACRONYM: GM

MEDLINETA: Org Lett

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