Reliable 13C NMR Method of Making Relative Stereochemical Assignments to Certain N-[α-Hetero-β-hydroxy(acetoxy)-β-(substituted phenyl)-1‘-oxopropyl]-2-oxazolidinones-Reference-Cited by-同舟云学术

Reliable 13C NMR Method of Making Relative Stereochemical Assignments to Certain N-[α-Hetero-β-hydroxy(acetoxy)-β-(substituted phenyl)-1‘-oxopropyl]-2-oxazolidinones

Published:1997-01-01 Issue:1 Volume:62 Page:216-220
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pridgen Lendon N.¹,De Brosse Charlie¹

Affiliation:

1. Synthetic Chemistry Department, Chemical, R&D, SmithKline & Beecham Pharmaceuticals Post Office Box 1539, King of Prussia, Pennsylvania 19406

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo951798l

Reference46 articles.

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2. Chelation control in metal-assisted aldol addition reactions of .alpha.-N-halogenated imide enolates leading to predominantly anti stereoselectivity. An example of a stereocontrolled Darzens reaction

3. A predominately anti-stereoselective chiral metal directed aldol condensation with aromatic aldehydes

4. Metal-assisted aldol condensation of chiral .alpha.-halogenated imide enolates: a stereocontrolled chiral epoxide synthesis

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