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Journal ArticleDOI

.alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

James A. Dale, +2 more
- 01 Sep 1969 - 
- Vol. 34, Iss: 9, pp 2543-2549
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This article is published in Journal of Organic Chemistry.The article was published on 1969-09-01. It has received 2312 citations till now. The article focuses on the topics: Reagent.

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Determination of the enantiomeric purity and the configuration of β-aminoalcohols using (R)-2-fluorophenylacetic acid (AFPA) and fluorine-19 NMR: application to β-blockers

TL;DR: In this paper, the enantiomeric purity and absolute configuration of β-aminoalcohols of type ArOCH2CH(OH)CH2NHR (R=iPr, tBu) were determined.
Journal ArticleDOI

Enantioselective synthesis of (R)-(−)-mevalonolactone via cyclic sulfate methodology

TL;DR: In this paper, an asymmetric synthesis of (R )-(−)-mevalonolactone is described using the Sharpless asymmetric dihydroxylation and the regioselective nucleophilic opening of a cyclic sulfate as key steps.
Journal ArticleDOI

Asymmetric [2+2] Cycloaddition Reaction Catalyzed by a Chiral Titanium Reagent

HayashiYujiro, +1 more
- 03 May 2006 - 
TL;DR: Asymmetric cycloaddition reaction between 3-(2-acryloyl)-1,3-oxazolidin-2-one derivatives and 1,1-bis(methylthio)ethylene proceeds by the use of a catalytic amount of a chiral titanium reagent to give the corresponding cyclobutanes in high enantioselectivity as discussed by the authors.
Journal ArticleDOI

The total syntheses of D-erythro-sphingosine, N-palmitoylsphingosine (ceramide), and glucosylceramide (cerebroside) via an azidosphingosine analog.

TL;DR: The cerebroside glucosylceramide (23) was the next sphingolipid in this series to be synthesized in a highly homogeneous form and was demonstrated to be optically pure by a novel method utilizing Mosher's acid.
Journal ArticleDOI

Acetals as chiral auxillaries Part 4 (1)

TL;DR: In this article, a precursor of the California Red scale pheromone has been prepared using BF 3 reagents associated with tributylphosphine, which react stereoselectivity with chiral α,β-ethylenic acetals.
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