Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groupsDirect synthesis of Z-alkenyl halides through catalytic cross-metathesisEnantioselective synthesis of P-stereogenic phosphinates and phosphine oxides by molybdenum-catalyzed asymmetric ring-closing metathesis.Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts.Synthesis of Tungsten Imido Alkylidene Complexes that Contain an Electron-Withdrawing Imido LigandSynthesis of Molybdenum and Tungsten Alkylidene Complexes That Contain Sterically Demanding Arenethiolate Ligands.Kinetically controlled E-selective catalytic olefin metathesis.Endo-selective enyne ring-closing metathesis promoted by stereogenic-at-W mono-pyrrolide complexes.Synthesis of (±)-tetrapetalone A-Me aglycon.Multifunctional organoboron compounds for scalable natural product synthesis.Catalytic Z-selective olefin cross-metathesis for natural product synthesis.Ethenolysis reactions catalyzed by imido alkylidene monoaryloxide monopyrrolide (MAP) complexes of molybdenum.Room Temperature Z-Selective Homocoupling of α Olefins by Tungsten CatalystsIsolation 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 metathesisZ-Selective olefin metathesis reactions promoted by tungsten oxo alkylidene complexesBipyridine Adducts of Molybdenum Imido Alkylidene and Imido Alkylidyne Complexes.Z-selective metathesis homocoupling of 1,3-dienes by molybdenum and tungsten monoaryloxide pyrrolide (MAP) complexesCatalytic enantioselective olefin metathesis in natural product synthesis. Chiral metal-based complexes that deliver high enantioselectivity and moreSimple organic molecules as catalysts for enantioselective synthesis of amines and alcoholsDipyrrolyl precursors to bisalkoxide molybdenum olefin metathesis catalystsMolybdenum Imido Alkylidene Metathesis Catalysts that Contain Electron Withdrawing Biphenolates or Binaphtholates.Diphenylamido Precursors to Bisalkoxide Molybdenum Olefin Metathesis Catalysts.The remarkable metal-catalysed olefin metathesis reaction.Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions.Inversion of configuration at the metal in diastereomeric imido alkylidene monoaryloxide monopyrrolide complexes of molybdenum.Highly efficient molybdenum-based catalysts for enantioselective alkene metathesisThree-component Ag-catalyzed enantioselective vinylogous mannich and Aza-Diels-Alder reactions with alkyl-substituted aldehydesSynthesis of High Oxidation State Molybdenum Imido Heteroatom-Substituted Alkylidene ComplexesZ-selective olefin metathesis processes catalyzed by a molybdenum hexaisopropylterphenoxide monopyrrolide complex.Highly Z-selective metathesis homocoupling of terminal olefins.Mo-catalyzed asymmetric olefin metathesis in target-oriented synthesis: enantioselective synthesis of (+)-africanol.An efficient, practical, and enantioselective method for synthesis of homoallenylamides catalyzed by an aminoalcohol-derived, boron-based catalystEnantioselective silyl protection of alcohols promoted by a combination of chiral and achiral Lewis basic catalysts.NHC-Cu-catalyzed addition of propargylboron reagents to phosphinoylimines. Enantioselective synthesis of trimethylsilyl-substituted homoallenylamides and application to the synthesis of S-(-)-cyclooroidin.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, amCatalytic SN2'- and Enantioselective Allylic Substitution with a Diborylmethane Reagent and Application in Synthesis.NHC-Cu-catalyzed protoboration of monosubstituted allenes. Ligand-controlled site selectivity, application to synthesis and mechanism.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.A multicomponent Ni-, Zr-, and Cu-catalyzed strategy for enantioselective synthesis of alkenyl-substituted quaternary carbons.
P50
Q28817194-A3412871-6E06-4112-90EF-F5C0B029E8A2Q29306760-B9FB7061-7347-4E2B-92E4-7263CFC91633Q33642215-A6163BD1-01A6-42B9-9F18-794952376656Q34268388-542D8DEE-17E4-482B-8435-200CF0497D29Q34331224-75FDC9B9-1DCB-4A8E-87CE-2B1E5B9F187FQ34331252-146D6D5C-449D-487B-B35D-3DF58CFD3914Q34524075-0B21DC12-6F28-44BB-BBFF-385021533712Q34574695-3409C5CA-D23C-4896-9071-7C0995275E27Q34660678-21E88797-7D16-45C2-88EC-A7FD8634D03AQ34712211-9DC12231-0625-404A-B96A-6AF951400870Q34858406-9476DFFA-627D-4FB9-A5C2-9C521D04EC7EQ34993073-06B4BC37-2F12-4424-BBDA-6CF31C4EE0D5Q35046796-137D36D4-72A7-4489-9063-85BE1050ADEDQ35131918-650E64D2-46EC-4AF6-9F1C-88181DAD554DQ35536355-5678A0A6-37C3-494F-A369-8710137E4B15Q35629403-D2B62740-63F5-426F-9362-AF1B1CA88CAEQ36157965-6EF7A207-E45C-419A-9B10-4D823C3974F8Q36157972-B39F2CD6-C069-4B87-912C-87F446700497Q36452747-E0296AE9-206C-4F15-A419-E659B8228628Q36620987-ED101B27-BFBB-494A-A378-5F58075EB685Q36859566-788DF914-A652-4291-94FE-845EC7C20924Q36946881-33DCB687-6F8C-4739-9E14-5265E601A4F9Q36979788-02AFB4F1-EBB3-4BF7-99CC-0AACC5E1EAAFQ36997705-86F6B725-148D-4E97-A997-703E115D01BCQ37118918-5872F3E1-896B-4143-9149-0589A3A0F44DQ37121099-92BBCCF0-166D-48A3-8F65-859B11F75365Q37146486-C8ABFA26-67F2-4291-8156-2F62AC94D17EQ37149448-B5DD5CFE-A38F-4FB5-AD33-5AB577BAE3B1Q37202254-A20365F8-797A-48B8-A37C-88555D2ECB55Q37262121-841FFE53-2C21-4217-9556-7B40C98A2A3CQ37457559-3E537EB0-3F59-4B23-A124-6115E0AC28BEQ37649256-740BA42B-B6CE-4D8E-984C-44C16BD2C65EQ37701450-4EDF5BF3-09E9-4528-B6FD-963B49468A08Q37726953-CD025251-8776-4932-ACBF-719A7A16F903Q38275026-45F1229E-05A2-404C-8272-2BA88EE2366BQ38919525-E940FF75-FB51-4D71-AE1E-19CFC7D49C1DQ39672627-0735D796-B803-49E5-AA65-5B7AD5E49653Q39834406-D84D3621-7AC0-4620-B75B-29FA1798C992Q39893077-814880F6-3364-4A7B-A682-FD506818E507Q40435109-AE11FACF-E27A-47BD-B5FA-79B527963D99
P50
description
Ameerika Ühendriikide keemik
@et
American chemist
@en
Amerikaans scheikundige
@nl
US-amerikanischer Chemiker
@de
Usana kemiisto
@io
amerikansk kemiker
@da
amerikansk kemist
@sv
amerikansk kjemikar
@nn
amerikansk kjemiker
@nb
chimist american
@ro
name
Amir H. Hoveyda
@af
Amir H. Hoveyda
@an
Amir H. Hoveyda
@ast
Amir H. Hoveyda
@bar
Amir H. Hoveyda
@br
Amir H. Hoveyda
@ca
Amir H. Hoveyda
@co
Amir H. Hoveyda
@cs
Amir H. Hoveyda
@cy
Amir H. Hoveyda
@da
type
label
Amir H. Hoveyda
@af
Amir H. Hoveyda
@an
Amir H. Hoveyda
@ast
Amir H. Hoveyda
@bar
Amir H. Hoveyda
@br
Amir H. Hoveyda
@ca
Amir H. Hoveyda
@co
Amir H. Hoveyda
@cs
Amir H. Hoveyda
@cy
Amir H. Hoveyda
@da
altLabel
Amir Hoveyda
@de
prefLabel
Amir H. Hoveyda
@af
Amir H. Hoveyda
@an
Amir H. Hoveyda
@ast
Amir H. Hoveyda
@bar
Amir H. Hoveyda
@br
Amir H. Hoveyda
@ca
Amir H. Hoveyda
@co
Amir H. Hoveyda
@cs
Amir H. Hoveyda
@cy
Amir H. Hoveyda
@da
P106
P21
P2381
P31
P373
Amir H. Hoveyda
P496
0000-0002-1470-6456
P569
1959-04-05T00:00:00Z