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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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A novel chiral auxiliary from chiral spiranes. cis,cis-(+)- and (–)-spiro[4.4]nonane-1,6-diol as chiral modifier in lithium aluminium hydride reduction of phenyl alkyl ketones

TL;DR: LiAlH4 reduction of phenyl alkyl ketones employing the hitherto unexplored chiral auxiliary cis,cis-(+)- and (−)-spiro[4.4]nonane-1,6-diol as chiral modifier gives the corresponding alcohol in 85-90% e.g. (enantiomeric excess).
Journal ArticleDOI

Conversion of Allylic Alcohols into Allylic Nitromethyl Compounds via a Palladium-Catalyzed Solvolysis: An Enantioselective Synthesis of an Advanced Carbocyclic Nucleoside Precursor1

TL;DR: A two-step reaction sequence to homoallylic nitro compounds from allylic alcohols is presented and serves as a centerpiece for the synthesis of an important carbocyclic nucleoside intermediate.
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Room-Temperature Metallation of 2-Substituted 1,3-Dithiane Derivatives and Subsequent Coupling with 2,3-Disubstituted Oxiranes

TL;DR: In this article, a mixture of mixed organometallic reagents, n-BuLi / Bu2Mg, was found to be an effective metallation reagent for 9 and the resulting anion reacted with 22 to afford the coupling product in good yield.
Journal ArticleDOI

Stereochemistry of Metabolism of Amphetamines: Use of (–)-α-Methoxy-α-(trifluoromethyl)phenylacetyl Chloride for GLC Resolution of Chiral Amines

TL;DR: The chiral acylating reagent was used in the determination of the enantiomeric composition of 2,5-dimethoxy-4- methylamphetamine excreted in rat urine after intraperitoneal drug administration and may be suitable for the resolution of amino acid enantiomers via the amide derivatives of the methyl esters.
Journal ArticleDOI

Polyphenols, Including the New Peapolyphenols A−C, from Pea Root Exudates Stimulate Orobanche foetida Seed Germination

TL;DR: Three new polyphenols, named peapolyphenols A-C, together with an already well-known polyphenol and a chalcone (1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphensyl)-1-propanone and 1,3-disubstituted propenone) were found to strongly stimulate Orobanche and Phelipanche species seed germination.
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