Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates.

Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Research Abstract Details 

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Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Abstract Text:

Franklin A Davis,Minsoo Song,

Syn-alpha-substituted beta-amino Weinreb amides are new chiral building blocks for asymmetric synthesis of syn-alpha-substituted beta-amino acids, aldehydes, and ketones and are prepared by addition of prochiral lithium enolates of Weinreb amides to sulfinimines (N-sulfinyl imines).

Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Publishing Authors By Initials

FA Davis,M Song,

For similar inorganic chemicals: sulfur compounds research abstracts see: inorganic chemicals: sulfur compounds research

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Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Journal Published:

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

Journal: Organic letters

VOLUME: 9

Page Numbers: 2413-6

Journal Abbreviation: Org. Lett.

ISSN: 1523-7060

DAY: 11

MONTH: 05

YEAR: 2007

Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Information

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LANGUAGE: eng

NlmUniqueID: 100890393

Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Keywords Mesh Terms:

KEYWORDS: Sulfur Compounds

MESH TERMS: chemistry

Chemical & Substance for Abstract: Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates. Information

Substance Name: Lithium

Registry Number: 7439-93-2

Grant and Affiliation Information for Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates.

AFFILIATION: Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, USA. fdavis@temple.edu

Country: United States

AGENCY: United States NIGMS

GRANT: GM 51982

ACRONYM: GM

MEDLINETA: Org Lett

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