about
Neutral chiral cyclopentadienyl Ru(ii)Cl catalysts enable enantioselective [2+2]-cycloadditions.Bis(imidate)palladium(II) complexes with labile ligands. Mimics of classical precursors?Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene.NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: (S,E)-ETHYL 6-(1,3-DIOXOLAN-2-YL)-4-METHYLHEX-2-ENOATE.Nickel-Catalyzed Alkyl-Alkyl Cross-Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent.Regio- and enantiospecific rhodium-catalyzed arylation of unsymmetrical fluorinated acyclic allylic carbonates: inversion of absolute configurationIridium(I)-Catalyzed Regio- and Enantioselective Allylic Amidation.Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalystsC-O hydrogenolysis catalyzed by Pd-PMHS nanoparticles in the company of chloroarenes.Synthesis of enantiomerically enriched imidazolidin-2-ones through asymmetric palladium-catalyzed alkene carboamination reactions.Reverse regioselectivity in the palladium(II) thiourea catalyzed intermolecular Pauson-Khand reaction.Iridium-catalyzed asymmetric ring-opening of azabicyclic alkenes with alcohols.Rhodium-catalyzed redox allylation reactions of ketones.Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines.Silver-catalyzed allenylation and enantioselective propargylation reactions of ketones.[RuCl₂(η⁶-p-cymene)] complexes bearing phosphinous acid ligands: preparation, application in C-H bond functionalization and mechanistic investigations.P-Trifluoromethyl ligands derived from Josiphos in the Ir-catalysed hydrogenation of 3,4-dihydroisoquinoline hydrochlorides.Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I).Mechanistic study on the palladium(II)-catalyzed synthesis of 2,3-disubstituted indoles under aerobic conditions: anion effects and the development of a low-catalyst-loading process.Anionic Palladium(0) and Palladium(II) Ate Complexes.Formation of a Trifluorophosphane Platinum(II) Complex by P-F Bond Activation of Phosphorus Pentafluoride with a Pt0 Complex.The Barbier-Grignard-type arylation of aldehydes using unactivated aryl iodides in water.Pd/C-Catalyzed Cyclizative Cross-Coupling of Two ortho-Alkynylanilines under Aerobic Conditions: Synthesis of 2,3'-Bisindoles.Ligand-enabled multiple absolute stereocontrol in metal-catalysed cycloaddition for construction of contiguous all-carbon quaternary stereocentres.Synthesis, structure and reactivity of a terminal magnesium fluoride compound, [TpBut,Me]MgF: hydrogen bonding, halogen bonding and C-F bond formation.Halide-Enhanced Catalytic Activity of Palladium Nanoparticles Comes at the Expense of Catalyst RecoveryThe Remarkable Effect of a Simple Ion: Iodide-Promoted Transfer Hydrogenation of Heteroaromatics
P2860
Q33679825-37C8DD28-F6B6-4BAD-B594-BE7FBCA85433Q33943336-882975CD-4662-4E3B-9A2C-AEDC0582C98BQ34746872-B5CE3093-EC50-4FF4-A42B-FBD078510580Q34999596-5453A4D0-05A9-4A04-B341-2A5910A30B29Q35907655-D90A880A-1E5E-47CF-BEA8-71F13ABD7CD7Q35928733-A26D7925-86C8-4001-9D70-1DB410CE38B4Q37238421-0FFDBD3E-ED8E-4F3F-B443-AF93849E85F7Q37681284-62F62A8C-E705-4204-A8F6-CBA2525B5FC2Q41846122-733B0000-90D5-4824-A9B6-75AB8944B620Q42396991-F7B58499-7D17-4DCA-9430-86788D99F28AQ44613156-CDFA4FD1-7950-437F-A5FB-79A446B1EF1BQ45277864-B29ABA0D-7FAD-4569-8ABA-50ABAF90E3AFQ45953220-E288F547-C359-4B9B-A69F-CC277BFADC36Q46507522-25BC272D-F02C-43D0-AC12-558C932DA63FQ46519730-43276E77-B5BC-46B7-AC65-D120AC045BBBQ46583562-A37C1C2D-6DD0-43FC-B4E0-3C7C269FC574Q46702654-4E018B52-0023-45F6-BC0F-7370D00B0D0BQ46819786-E4626876-688C-45DC-8E99-1852353C7831Q46853925-AFCAD7BB-4B6E-4554-A981-4EECA22BC092Q48222899-F774FEF0-9FD6-4D8A-A071-1A40E9FFBB97Q48245654-F1D78C70-853E-43E7-8216-1B43D9714B4EQ50453888-4635A62D-C651-4878-B14F-1133934388B9Q53277558-B0E90EF5-8495-4142-97F6-5FE9743247F3Q54428367-4C5DB972-9B53-46E5-BF46-07ADB5F4C530Q54959210-898ABE81-7E06-4956-9AB2-8ECBBB13BD42Q57871287-F855C823-5AEF-4ABE-8122-CBB75033D98AQ58376126-5DA9A884-3C26-4707-963B-27CDA00DA4C6
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Halide effects in transition metal catalysis.
@ast
Halide effects in transition metal catalysis.
@en
type
label
Halide effects in transition metal catalysis.
@ast
Halide effects in transition metal catalysis.
@en
prefLabel
Halide effects in transition metal catalysis.
@ast
Halide effects in transition metal catalysis.
@en
P2860
P1433
P1476
Halide effects in transition metal catalysis.
@en
P2093
Keith Fagnou
Mark Lautens
P2860
P356
10.1002/1521-3773(20020104)41:1<26::AID-ANIE26>3.0.CO;2-9
P577
2002-01-01T00:00:00Z