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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 new method for the enantioselective synthesis of N-Boc-α,α-disubstituted α-amino acids

TL;DR: In this paper, a new method for the enantioselective synthesis of N-Boc-α,α-disubstituted α-amino acids has been developed.
Journal ArticleDOI

A convergent strategy towards taxol. A facile enantioselective entry into a fully functionalized ring A system

TL;DR: In this paper, the taxol ring A system has been synthesized in enantiomerically pure form by a short and efficient route featuring a Diels-Alder reaction and a Corey oxazaborolidine reduction.
Journal ArticleDOI

Asymmetric Synthesis of the Both Enantiomers of α-Hydroxy Acids by the Diastereoselective Reduction of Chiral α-Keto Amides with (Complex) Metal Hydrides in the Presence of Metallic Salt

TL;DR: In this article, the effects of the metallic salts and the reducing reagents in the diastereoselective reduction of chiral α-keto amides derived from (S)-proline methyl ester were examined.
Journal ArticleDOI

Substrate specificity and enantioselectivity of penicillinacylase catalyzed hydrolysis of phenacetyl esters of synthetically useful carbinols

TL;DR: Penicillinacylase from Ecoli, immoblized on Eupergit C beads catalyzes the hydrolysis in water/CH 3 CN 10:1, at pH 75 and 23° C, of a set of O-phenylacetate esters of primary carbinols as discussed by the authors.
Journal ArticleDOI

Stereoselective Synthesis of Highly Functionalized Cyclopropanes. Application to the Asymmetric Synthesis of (1S,2S)-2,3-Methanoamino Acids

TL;DR: Molecular mechanics calculations using a modified MM2 type force field adapted to the pi-allyl palladium complexes have explained the reversibility of the palladium-catalyzed cyclization step, responsible for the low enantioselectivity observed and for the formation of byproducts, i.e., azepine derivatives 8a,b arising from subsequent aza Cope ring expansion.
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