Catalytic Z-selective olefin cross-metathesis for natural product synthesis. - Wikidata - wikimedia - TriplyDB

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

http://www.wikidata.org/entity/Q34858406

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Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis Ring-closing metathesis reactions: interpretation of conversion-time data."Black Swan events" in organic synthesis.Synthesis of Tungsten Imido Alkylidene Complexes that Contain an Electron-Withdrawing Imido Ligand Synthesis of Molybdenum and Tungsten Alkylidene Complexes That Contain Sterically Demanding Arenethiolate Ligands.Ru-Based Z-Selective Metathesis Catalysts with Modified Cyclometalated Carbene Ligands.Kinetically controlled E-selective catalytic olefin metathesis.Functionalized olefin cross-coupling to construct carbon-carbon bonds.Chelated ruthenium catalysts for Z-selective olefin metathesis.Isolation of pure disubstituted E olefins through Mo-catalyzed Z-selective ethenolysis of stereoisomeric mixtures.Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis Z-Selective olefin metathesis reactions promoted by tungsten oxo alkylidene complexes Decomposition pathways of Z-selective ruthenium metathesis catalysts Bipyridine Adducts of Molybdenum Imido Alkylidene and Imido Alkylidyne Complexes.Z-selective metathesis homocoupling of 1,3-dienes by molybdenum and tungsten monoaryloxide pyrrolide (MAP) complexes Z-Selective ethenolysis with a ruthenium metathesis catalyst: experiment and theory New indenylidene-type metathesis catalysts bearing unsymmetrical N-heterocyclic ligands with mesityl and nitrobenzyl substituents.Synthesis of High Oxidation State Molybdenum Imido Heteroatom-Substituted Alkylidene Complexes Investigations into Ruthenium Metathesis Catalysts with Six-Membered Chelating NHC Ligands: Relationship between Catalyst Structure and Stereoselectivity.A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps.Neurotrophic natural products: chemistry and biology.General approach to the synthesis of the chlorosulfolipids danicalipin A, mytilipin A, and malhamensilipin A in enantioenriched form.Chemical synthesis of the cardiotonic steroid glycosides and related natural products.Asymmetric catalysts for stereocontrolled olefin metathesis reactions.Efficient and selective formation of macrocyclic disubstituted Z alkenes by ring-closing metathesis (RCM) reactions catalyzed by Mo- or W-based monoaryloxide pyrrolide (MAP) complexes: applications to total syntheses of epilachnene, yuzu lactone, am Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity.Carboxylate-assisted C(sp³)-H activation in olefin metathesis-relevant ruthenium complexes.Catalytic, enantioselective synthesis of 1,2-anti-diols by asymmetric ring-opening/cross-metathesis.Improved ruthenium catalysts for Z-selective olefin metathesis Evolution of catalytic stereoselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity.Synthesis of Z-(pinacolato)allylboron and Z-(pinacolato)alkenylboron compounds through stereoselective catalytic cross-metathesis.Tandem Olefin Metathesis/Oxidative Cyclization: Synthesis of Tetrahydrofuran Diols from Simple Olefins.Catalyst-controlled stereoselective olefin metathesis as a principal strategy in multistep synthesis design: a concise route to (+)-neopeltolide.Control of olefin geometry in macrocyclic ring-closing metathesis using a removable silyl group.Alkene chemoselectivity in ruthenium-catalyzed Z-selective olefin metathesis.Approaches to the chemical synthesis of the chlorosulfolipids.Z-selective homodimerization of terminal olefins with a ruthenium metathesis catalyst.Preparation of macrocyclic Z-enoates and (E,Z)- or (Z,E)-dienoates through catalytic stereoselective ring-closing metathesis Molybdenum-based complexes with two aryloxides and a pentafluoroimido ligand: catalysts for efficient Z-selective synthesis of a macrocyclic trisubstituted alkene by ring-closing metathesis Enol ethers as substrates for efficient Z- and enantioselective ring-opening/cross-metathesis reactions promoted by stereogenic-at-Mo complexes: utility in chemical synthesis and mechanistic attributes.

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Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

http://www.wikidata.org/entity/Q34858406

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

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name

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@ast

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@en

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@nl

type

label

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@ast

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@en

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@nl

prefLabel

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@ast

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@en

Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@nl

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Catalytic Z-selective olefin cross-metathesis for natural product synthesis.

@en

P2093

Josep Llaveria

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Robert V O'Brien

http://www.w3.org/2001/XMLSchema#string

Simon J Meek

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P2860

CD1d-lipid-antigen recognition by the semi-invariant NKT T-cell receptor

Plasmalogens: biosynthesis and functions

Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts.

Catalytic enantioselective olefin metathesis in natural product synthesis. Chiral metal-based complexes that deliver high enantioselectivity and more

The remarkable metal-catalysed olefin metathesis reaction.

Highly efficient molybdenum-based catalysts for enantioselective alkene metathesis

Highly Z-selective metathesis homocoupling of terminal olefins.

Endo-selective enyne ring-closing metathesis promoted by stereogenic-at-Mo monoalkoxide and monoaryloxide complexes. Efficient synthesis of cyclic dienes not accessible through reactions with Ru carbenes.

Vicinal diboronates in high enantiomeric purity through tandem site-selective NHC-Cu-catalyzed boron-copper additions to terminal alkynes.

The significance of degenerate processes to enantioselective olefin metathesis reactions promoted by stereogenic-at-Mo complexes.

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461-466

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scholarly article

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10.1038/NATURE09957

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7339

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471

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Richard R. Schrock

Amir H. Hoveyda

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2011-03-01T00:00:00Z

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50832121

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1044829242

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21430774

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3082443

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