About: The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scholarly article by Karl Barry Sharpless et al published May 1992 in Journal of Organic Chemistry

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1992 (uk) article scientifique publié en 1992 (fr) im Mai 1992 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Karl Barry Sharpless et al published May 1992 in Journal of Organic Chemistry (en)
publication date	wds:Q55968533-ED42A06E-2D40-480B-B5E7-FE6ED5C4BF22
publication date	1992-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55968533-AB7C65F3-DBB4-46AB-AA66-C3D41CBDA390
language of work or name	English
author name string	wds:Q55968533-361D6F0C-669C-49C3-948C-95F7CD97B918 wds:Q55968533-977BBECE-C140-4A2B-99D1-B899608B2F2E wds:Q55968533-995F677C-D315-429D-A050-81BCC3182251 wds:Q55968533-9D72BEDE-E53A-448E-9FE1-77F38757F7DF wds:Q55968533-BF21223C-3CD6-4E91-97E4-54C1DF274C2D wds:Q55968533-FCB865A6-DABC-496B-AB18-B40C28D56550 wds:Q55968533-FE834059-0707-4C11-93A9-09E840112F1D
author name string	Jens Hartung Youssef L. Bennani Gerard A. Crispino Hoi Lun Kwong Kouhei Morikawa Willi Amberg Zhi Min Wang
rdfs:label	The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (en) The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (nl)
skos:prefLabel	The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (en) The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (nl)
name	The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (en) The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (nl)
author	wds:Q55968533-7AA7F83B-4038-4CBF-BE85-8152F803506A wds:Q55968533-F1482DA7-B9AC-4A54-9F7D-2FBCE3E4DC71
author	Karl Barry Sharpless Kyu-Sung Jeong
title	wds:Q55968533-F5DE0BE7-BE71-4159-96CB-B16A473BA2A6
title	The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement (en)
page(s)	wds:Q55968533-939666FB-A666-4F80-BC4D-687FA38D7905
page(s)	2768-2771
instance of	wds:Q55968533-F78EDEAE-FC6E-4FCC-86A8-16E2D89C1BFE
instance of	scholarly article
main subject	wds:Q55968533-5F7BD1D1-C798-4F62-8E1E-5FBE6C057BE2
main subject	osmium
published in	wds:Q55968533-3089AE8D-4138-4E71-AF2E-03706C24C2EA
published in	Journal of Organic Chemistry
issue	wds:Q55968533-BD137CC7-1E50-4E08-9BEF-2B2DD649DE66
volume	wds:Q55968533-E446B224-257F-43DF-9098-42E1C1DB8F7A
issue	10
volume	57
DOI	wds:Q55968533-7FD86A83-FE4F-4B04-ADBF-429AB030156E
DOI	http://dx.doi.org/10.1021/JO00036A003
DOI	10.1021/JO00036A003
ResearchGate publication ID	wds:Q55968533-4FB2F5F0-BED4-4E78-82EF-4B9A161A8D00
ResearchGate publication ID	231567906
Mendeley publication ID	wds:Q55968533-D8FE04E7-A569-47E8-8CB0-16B999E768E1
Mendeley publication ID	efce1967-a7d0-3f04-bec0-2fbed9d341ec
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55968533
is cites work of	Design and synthesis of a new sialyl Lewis X mimetic: how selective are the selectin receptors? Anti-AIDS agents. 33. Synthesis and anti-HIV activity of mono-methyl substituted 3',4'-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK) analogues Metal-catalysed 1,2-diamination reactions The orphan nuclear receptor LXRalpha is positively and negatively regulated by distinct products of mevalonate metabolism On the use of C2-symmetric aziridines as chiral auxiliaries Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside Dimeric Cinchona alkaloids X-ray crystallographic studies provide additional evidence that an enzyme-like binding pocket is crucial to the enantioselective dihydroxylation of olefins by OsO4—bis-cinchona alkaloid complexes A kinetic and thermodynamic study of the unexpected comproportionation reaction between cis-[Os(VIII)O4(OH)2](2-) and trans-[Os(VI)O2(OH)4](2-) to form a postulated [Os(VII)O3(OH)3](2-) complex anion Microbiological transformations. Part 46: Preparation of enantiopure (S)-2-pyridyloxirane via epoxide hydrolase-catalysed kinetic resolution Determination of the stereochemistry of the aggregation pheromone of harlequin bug, Murgantia histrionica LEDGINs, non-catalytic site inhibitors of HIV-1 integrase: a patent review (2006 - 2014). An improved synthesis of (20R,22R)-cholest-5-ene-3beta,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR alpha Synthesis of the first enantiomerically pure and chiral, disubstituted 3,4-ethylenedioxythiophenes (EDOTs) and corresponding stereo- and regioregular PEDOTs Asymmetric synthesis of novel quaternary alpha-hydroxy-delta-lactam dipeptide surrogates Studies toward the total synthesis of pluraflavin A The Quest for Quinine: Those Who Won the Battles and Those Who Won the War A new cationic, chiral catalyst for highly enantioselective Diels-Alder reactions Toward an Understanding of the High Enantioselectivity in the Osmium-Catalyzed Asymmetric Dihydroxylation. 4. Electronic Effects in Amine-Accelerated Osmylations Total synthesis of kaitocephalin, the first naturally occurring AMPA/KA receptor antagonist Synthesis and bioactivity of natural and C-3 fluorinated biosynthetic precursors of 28-homobrassinolide Enantioselective total synthesis of (+)-brazilin, (-)-brazilein and (+)-brazilide A. Metal-Catalyzed Asymmetric Michael Addition in Natural Product Synthesis Tandem Z-Selective Cross-Metathesis/Dihydroxylation: Synthesis of anti-1,2-Diols The truth about false unicorn (Chamaelirium luteum): total synthesis of 23R,24S-chiograsterol B defines the structure and stereochemistry of the major saponins from this medicinal herb. Biotransformations with Rhizopus arrhizus and Geotrichum candidum for the preparation of (S)-atenolol and (S)-propranolol Ruthenium-catalyzed selective monoamination of vicinal diols. Enantioselective synthesis and antioxidant activity of 3-(3,4-dihydroxyphenyl)-glyceric acid--basic monomeric moiety of a biologically active polyether from Symphytum asperum and S. caucasicum Combating cholesterol Radical cyclization of beta-alkoxyacrylates: synthesis of a C2-symmetric, L-shaped molecule with four fused tetrahydropyran rings Synthetic studies on himbacine, a potent antagonist of the muscarinic M2 subtype receptor. Part 2: synthesis and muscarinic M2 subtype antagonistic activity of the novel himbacine congeners modified at the C-3 position of lactone moiety Highly effective transition structure designed catalyst for the enantio- and position-selective dihydroxylation of polyisoprenoids Dearomative dihydroxylation with arenophiles. Total synthesis of (+)-macrosphelides A, C, E, F, and G based on enzymatic function Total synthesis of isotopically labelled flavonoids. Part 3: † †For Part 2, see Ref. 1. 13 C-labelled (−)-procyanidin B3 from 1-[ 13 C]-acetic acid Selective perhydroxylation of squalene: taming the arithmetic demon Combined NK1 and NK2 tachykinin receptor antagonists: synthesis and structure-activity relationships of novel oxazolidine analogues Oxidation of 3-C-(2-amino-2-deoxy-D-glucopyranosyl)-1-propene compounds and the structure of 3-C-(2-amino-2-deoxy-D-glucopyranosyl)-1,2-propanediol derivatives for a synthesis of 2,3-didehydro-2,7-dideoxy-N-acetylneuraminic acid Asymmetric Dihydroxylation of Alkenes Convenient route to derivatives of the 2-deoxysugar subunits of the kedarcidin chromophore: L-mycarose and L-kedarosamine Updating the asymmetric osmium-catalyzed dihydroxylation (AD) mnemonic: Q2MM modeling and new kinetic measurements Total synthesis of bryostatins: the development of methodology for the atom-economic and stereoselective synthesis of the ring C subunit Recent applications of Cp2TiCl in natural product synthesis Selective Synthesis of Chiral Dioxabicyclo[4.4.0]decane and Dioxabicyclo[5.3.0]decane from 3,4-Bisallyloxy-but-1-yne Derivatives via Ruthenium-Catalyzed En-yn-ene Metathesis

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software