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Molecular Models of Products and Reactants from an Asymmetric Synthesis of a Chiral Carboxylic Acid

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William F. Coleman

Department of Chemistry, Wellesley College, Wellesley, MA 02481

J. Chem. Educ., 2008, 85 (5), p 752

DOI: 10.1021/ed085p752

Publication Date (Web): May 1, 2008

Abstract

The Featured Molecules for this month are based on the use of 4-benzyl-2-oxazolidinone in the synthesis of a chiral carboxylic acid and include 4-dimethylaminopyridine, sodium bis(trimethylsilyl)amide, chelated (Z)-enolate of N-propionyl oxazolidinone, allyl iodide, andallylated oxazolidinone.

Keywords (Audience):

Second-Year Undergraduate

Keywords (Domain):

Organic Chemistry

Keywords (Feature):

JCE Featured Molecules

Keywords (Pedagogy):

Computer-Based Learning

Keywords (Subject):

Molecular Modeling

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Citing Articles

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This article has been cited by 1 ACS Journal articles (1 most recent appear below).

Reflecting on 103 Months of Featured Molecules
William F. Coleman
Journal of Chemical Education2010 87 (12), 1458-1459
- Reflecting on 103 Months of Featured Molecules
  William F. Coleman
  Journal of Chemical Education2010 87 (12), 1458-1459
  This is the 103rd and final article in the JCE Featured Molecules column under the guidance of William F. Coleman. The goal of the Featured Molecules column since its first appearance in 2002 has been to add a third dimension to many of the chemical ...
  Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links