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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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Purification and characterization of two oxidoreductases involved in the enantioselective reduction of 3-oxo, 4-oxo and 5-oxo esters in baker's yeast

TL;DR: Two NADPH-dependent oxidoreductases catalyzing the enantioselective reduction of 3-oxo esters to (S)- and (R)-3-hydroxy acid esters have been purified 121- and 332-fold from cell extracts of Saccharomyces cerevisiae.
Journal ArticleDOI

Asymmetric Diels‐Alder Reactions of Neopentyl‐Ether‐Shielded Acrylates and Allenic Esters: Syntheses of (−)‐Norbornenone and (−)‐β‐Santalene

TL;DR: In this article, a cycloaddition of cyclopentadiene to allenic ester with 95 % endo-and 99.2% πpH-face selectivities was proposed.
Journal ArticleDOI

A novel approach to the synthesis of optically pure non protein α-amino acids in both L and D configurations from L-serine

TL;DR: In this paper, the (2R)-2-Boc-amino-3-phenylsulfonyl-l-propanol 3 and its enantiomer 9 from L-serine are described.
Journal ArticleDOI

Enantioselective conjugate addition to cyclic enones with scalemic lithium organo(amido)cuprates, Part IV. Relationship between ligand structure and enantioselectivity

TL;DR: In this paper, the most successful chiral ligand is (S)-N-methyl-1-phenyl-2-(1-piperidinyl)ethanamine, 13, which reacts with cyclic enones to form products with up to 97% ee.
Journal ArticleDOI

Mangicols: Structures and Biosynthesis of A New Class of Sesterterpene Polyols from a Marine Fungus of the Genus Fusarium

TL;DR: A marine fungal isolate, tentatively identified as Fusarium heterosporum, has been found to produce a series of structurally novel sesterterpene polyols, the mangicols A-G, which show only weak to modest cytotoxicities toward a variety of cancer cell lines in in vitro testing.
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