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Journal ArticleDOI

New ligands double the scope of the catalytic asymmetric dihydroxylation of olefins

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TLDR
Improved ligands render terminal olefins good substrates for the osmium-catalyzed asymmetric dihydroxylation (ADH) process as discussed by the authors.
Abstract
Improved ligands render terminal olefins good substrates for the osmium-catalyzed asymmetric dihydroxylation (ADH) process, and the amounts of chiral ligand and osmium catalyst required diminish dramatically

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Citations
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Journal ArticleDOI

The first synthesis of vancomycinic acid

TL;DR: Vancomycinic Acid moiety (C, D and E rings) 2 of vancomYcin is synthesised making efficient use of the ease of nucleophilic displacements of halides on 2,6-dibromobenzoquinone followed by a diastereoselective elaboration of the quinone unit to aryl glycine.

Chemistry and Biology of Cinchona Alkaloids 21

TL;DR: Cinchona alkaloids comprising quinine, quinidine, cinchonidine, and Cinchonine as the major members constitute a unique class of quinoline alkaloid with tremendous impact on human civilization as mentioned in this paper.
Book ChapterDOI

Proanthocyanidins: Chemistry and Biology

TL;DR: In this article, the authors summarized progress in the chemistry and biology of the proanthocyanidins, a diverse group of naturally occurring plant polyphenols, emphasizing results emanating from studies in the post-CONAP-I era.
Journal ArticleDOI

Diastereocontrol in the asymmetric dihydroxylation of chiral 3-alkenyl-4,5-dihydroisoxazoles

TL;DR: In this paper, the authors show that, in the case of catalytic asymmetric dihydroxylation of 4, one diastereomer was heavily predominant with (DHQ)2-PHAL as the chiral auxiliary (mismatched pair; 90% d.e.
References
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PatentDOI

First practical method for asymmetric epoxidation

TL;DR: In this article, a metal alkoxide is used as a catalyst, where the metal has a coordination number of at least four, and at least one, usually two, of the alkoxide groups bonded to the metal are bonded to asymmetric carbon atoms.
Journal ArticleDOI

Asymmetric dihydroxylation via ligand-accelerated catalysis

TL;DR: Dihydroxylation asymetrique de composes ethyleniques du type styrene, vinylcyclohexane, hexene-3 en les glycols correspondants as mentioned in this paper.
Journal ArticleDOI

An improved synthesis of the taxol side chain and of RP 56976

TL;DR: In this paper, the methode presentee se fait au depart de phenyl-3 dihydroxy-2,3 propionate de methyle via epoxydation, et d'azoture de sodium.
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