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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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Synthesis of medium ring ethers. Part 4. Stereoselective Claisen-mediated ring expansion as a route to homochiral disubstituted medium ring lactones

TL;DR: In this article, the selenoxides derived from the enantiomerically pure phenylselenomethyl-substituted cyclic acetals 4 and 8 proceeds stereospecifically to provide the homochiral 8- and 7-membered lactones 5 and 9 respectively.
Journal ArticleDOI

Optically Pure Isoproterenol Analogues With Side Chains Containing an Amide Bond: Synthesis and biological properties

TL;DR: Both ( 6R,2′R)-4a and (6R, 2′R-4b) show long lasting positive inotropic activity after intravenous as well as oral administration and are at least three times as potent as rac-isoproterenol.
Journal ArticleDOI

Conversion of chiral amino acids to enantiomerically pure α-methylamines

B. G. Donner
- 20 Feb 1995 - 
TL;DR: In this article, anantiomerically enriched α-methylamines are obtained in high yield by Raney nickel reduction of N-Boc-protected, amino acid-derived thioethers.
Journal ArticleDOI

Chiral organosilicon compounds in synthesis: Regio and stereoselective alkylation of a chiral α-silylcinnamyl carbanion

TL;DR: Good regio- and stereoselectivity can be obtained in the alkylation of chiral α-silylcinnamyl carbanion 8 in toluene as mentioned in this paper.
Journal ArticleDOI

Stereoselectivity of the carbonyl reduction of dolasetron in rats, dogs, and humans

TL;DR: Enantioselectivity was not due to differences in the absorption, distribution, metabolism, or excretion of enantiomers, as iv or oral administration of rac-reduced dolasetron to rats and dogs lead to the recovery of essentially the same enantiomeric composition as the dose administered.
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