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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Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural ProductSynthesis of Tungsten Imido Alkylidene Complexes that Contain an Electron-Withdrawing Imido LigandRu-Based Z-Selective Metathesis Catalysts with Modified Cyclometalated Carbene Ligands.Development of Chiral Bis-hydrazone Ligands for the Enantioselective Cross-Coupling Reactions of Aryldimethylsilanolates.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) complexesSynthesis of High Oxidation State Molybdenum Imido Heteroatom-Substituted Alkylidene ComplexesEfficient 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, amStereoretentive 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.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.Catalyst-controlled stereoselective olefin metathesis as a principal strategy in multistep synthesis design: a concise route to (+)-neopeltolide.Alkene chemoselectivity in ruthenium-catalyzed Z-selective olefin 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 metathesisEnantioselective olefin metathesis with cyclometalated ruthenium complexes.Catalytic Z-selective cross-metathesis with secondary silyl- and benzyl-protected allylic ethers: mechanistic aspects and applications to natural product synthesis.Highly Z-selective and enantioselective ring-opening/cross-metathesis catalyzed by a resolved stereogenic-at-Ru complex.Stereoselective access to Z and E macrocycles by ruthenium-catalyzed Z-selective ring-closing metathesis and ethenolysis.Ruthenium carbenes supported on mesoporous silicas as highly active and selective hybrid catalysts for olefin metathesis reactions under continuous flow.Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.
P2860
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P2860
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.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Enol ethers as substrates for ...... is and mechanistic attributes.
@en
Enol ethers as substrates for ...... is and mechanistic attributes.
@nl
type
label
Enol ethers as substrates for ...... is and mechanistic attributes.
@en
Enol ethers as substrates for ...... is and mechanistic attributes.
@nl
prefLabel
Enol ethers as substrates for ...... is and mechanistic attributes.
@en
Enol ethers as substrates for ...... is and mechanistic attributes.
@nl
P2093
P2860
P356
P1476
Enol ethers as substrates for ...... is and mechanistic attributes.
@en
P2093
Ismail Ibrahem
Masayuki Hasegawa
P2860
P304
P356
10.1021/JA210946Z
P407
P577
2012-01-24T00:00:00Z