The heck reaction as a sharpening stone of palladium catalysis.
about
Strategic Application of Residence-Time Control in Continuous-Flow ReactorsC-C coupling of N-heterocycles at the fac-Re(CO)(3) fragment: synthesis of pyridylimidazole and bipyridine ligands.A Family of Potent Ru(II) Photosensitizers with Enhanced DNA Intercalation: Bimodal Photokillers.Diaminocarbene- and Fischer-carbene complexes of palladium and nickel by oxidative insertion: preparation, structure, and catalytic activity.Sequential Cu(I)/Pd(0)-catalyzed multicomponent coupling and annulation protocol for the synthesis of indenoisoquinolines.Enantioselective construction of remote quaternary stereocentresPalladium-Catalyzed Enantioselective Heck Alkenylation of Trisubstituted Allylic Alkenols: A Redox-Relay Strategy to Construct Vicinal StereocentersPd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational studyAllylic functionalization of unactivated olefins with Grignard reagents.Air/Water-Stable Tridentate NHC-Pd Complex; Catalytic C-H Activation of Hydrocarbons via H/D Exchange Process in D(2)O.Synthesis of N-Aryl-2-allyl Pyrrolidines via Palladium-catalyzed Carboamination Reactions of γ-(N-Arylamino)alkenes with Vinyl Bromides.Palladium-catalyzed oxidative intermolecular difunctionalization of terminal alkenes with organostannanes and molecular oxygenPd(II)-catalyzed oxidative 1,1-diarylation of terminal olefins.Development of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactonesCationic Pd(II)-catalyzed Fujiwara-Moritani reactions at room temperature in water.Transmetallation versus β-hydride elimination: the role of 1,4-benzoquinone in chelation-controlled arylation reactions with arylboronic acids.Synthesis of heterocycles via Pd-ligand controlled cyclization of 2-chloro-N-(2-vinyl)aniline: preparation of carbazoles, indoles, dibenzazepines, and acridines.Pd(II) conjugated chitosan nanofibre mats for application in Heck cross-coupling reactions.Simplifying nickel(0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenesMicrowave and continuous flow technologies in drug discovery.A highly selective and general palladium catalyst for the oxidative Heck reaction of electronically nonbiased olefins.A palladium-catalyzed three-component cross-coupling of conjugated dienes or terminal alkenes with vinyl triflates and boronic acidsFunctionalized Poly(3-hexylthiophene)s via Lithium-Bromine ExchangeBreaking the regioselectivity rule for acrylate insertion in the Mizoroki-Heck reaction.Halide effects in transition metal catalysis.Operationally simple and highly (E)-styrenyl-selective Heck reactions of electronically nonbiased olefins.Highly selective coupling of alkenes and aldehydes catalyzed by [Ni(NHC){P(OPh)3}]: synergy between a strong sigma donor and a strong pi acceptorNickel-Catalyzed Coupling Reactions of AlkenesNickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates.Catalytic Addition of Simple Alkenes to Carbonyl Compounds Using Group 10 MetalsDeveloping piperine towards TRPV1 and GABAA receptor ligands--synthesis of piperine analogs via Heck-coupling of conjugated dienes.Aryliodine (III) Diacetates as Substrates for Pd-Ag Catalyzed Arylation of Alkenes.Combination of microwave reactions with fluorous separations in the palladium-catalyzed synthesis of aryl sulfidesCopper-catalyzed enantioselective intramolecular alkene amination/intermolecular Heck-type coupling cascade.Palladium-Catalyzed Cross-Coupling of α-Bromocarbonyls and Allylic Alcohols for the Synthesis of α-Aryl Dicarbonyl Compounds.Relative reactivity of alkenyl alcohols in the palladium-catalyzed redox-relay Heck reaction.Palladium-catalyzed β-(hetero)arylation of α,β-unsaturated valerolactams.Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols.Palladium(II)-catalyzed enantio- and diastereoselective synthesis of pyrrolidine derivativesCatalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions.
P2860
Q26801617-8F6BC296-370F-4079-AC4D-8F672A43B7D9Q30791394-05FBD9CA-938B-47D1-8194-BD7B9CBF8433Q30977137-F6D48DDC-1EA7-4ACC-898E-4F4BA0744D0FQ31144230-41D6C48F-C3AA-4D6E-8325-9E4FF334709DQ33401654-EB5FBEF1-F59F-4C86-A286-D850541F82A1Q33554259-4FD2E9E2-C47E-49F8-838D-5770C8F2C098Q33574701-A9029B6D-3221-4128-BD49-F69ED9DA7BE6Q33586499-B04EFD1D-0B87-4082-9565-7C9A23636E96Q33684656-21886D42-1D13-460A-8309-15D10956C1F0Q33714201-6AA7BF11-190D-4023-87A8-4F1DB3BF6BC0Q33714654-5099AC7C-FBC4-44FA-ABC9-BF2AA33161AFQ33750247-E86D018A-905B-4750-84F5-66F55B37DEC4Q34015488-D4D3AA31-F66E-4B82-9B29-9B53D20D4AF0Q34073280-0DC87102-E386-4F55-AD0F-5FEACC5A9572Q34108251-E7603216-9CC1-4A10-B412-B645BADBB06BQ34178015-3294A06D-6888-4552-B2AA-34FD6DB2AE7EQ34183000-E52009B2-6F34-43A7-9478-6ECAD9CCF600Q34225613-A93C737E-BD4F-4258-8894-CB0587934750Q34322450-800F1760-EAC0-416F-8732-ED60ED7E1946Q34419675-CE5CF5CD-33BE-4B8A-AA82-6EABAC8112C9Q34446745-B7BD7CF7-962F-40BA-8530-619EB60B0F3BQ34887998-BFB11714-E12E-437F-8096-B689AF48E5A6Q34972477-54E5C1A7-C186-4696-89CB-2F68AFABF86CQ35022095-A9E7F2D5-327E-45DC-8955-E4C998AAA9EEQ35030211-7EC65669-77F3-4559-998A-55AE22775623Q35070577-0701349F-BA97-44F0-B00F-AB654E08332AQ35141058-D149D868-A79D-46C9-8A46-15E6192F712FQ35141061-868C4FAA-BC3D-4035-86A5-C486CD397B35Q35141081-54CA6A30-4BE4-4B0F-841F-21F9437435D0Q35197033-7A1E18DD-130D-488F-A680-C4C7F1C167D1Q35463986-28F2B717-920C-4BD5-A086-DAF67C1F29F7Q35499155-62922F47-2F6B-4AC5-9890-790E986CE170Q35847156-83EFF7B7-9410-4444-AE2E-F80131FB09B9Q35857570-C6D23BA2-8D74-4EC0-876C-95C2619FA442Q35892352-39045DA5-2B8B-4136-9FAB-B908C142661BQ36069302-ECDB7E44-9147-463B-B7E3-6E70CA33C0E3Q36086854-0068A6C8-1DDC-47DB-BF63-2E71F5C4035BQ36168244-EACAD390-0964-428D-8063-6100A246DACFQ36282903-0765D296-8F01-4F65-ABE5-FE956FEF434AQ36392607-075E656D-F251-4932-BFA3-407752509643
P2860
The heck reaction as a sharpening stone of palladium catalysis.
description
2000 nî lūn-bûn
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2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
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2000 թվականի օգոստոսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
The heck reaction as a sharpening stone of palladium catalysis.
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The heck reaction as a sharpening stone of palladium catalysis.
@en
The heck reaction as a sharpening stone of palladium catalysis.
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type
label
The heck reaction as a sharpening stone of palladium catalysis.
@ast
The heck reaction as a sharpening stone of palladium catalysis.
@en
The heck reaction as a sharpening stone of palladium catalysis.
@nl
prefLabel
The heck reaction as a sharpening stone of palladium catalysis.
@ast
The heck reaction as a sharpening stone of palladium catalysis.
@en
The heck reaction as a sharpening stone of palladium catalysis.
@nl
P356
P1433
P1476
The heck reaction as a sharpening stone of palladium catalysis.
@en
P2093
A V Cheprakov
I P Beletskaya
P304
P356
10.1021/CR9903048
P577
2000-08-01T00:00:00Z