About: PEPPSI-Type Palladium Complexes Containing Basic 1,2,3-Triazolylidene Ligands and Their Role in Suzuki-Miyaura Catalysis

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About: PEPPSI-Type Palladium Complexes Containing Basic 1,2,3-Triazolylidene Ligands and Their Role in Suzuki-Miyaura Catalysis Goto Sponge NotDistinct Permalink

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scholarly article by Daniel Canseco-Gonzalez et al published 29 March 2012 in Chemistry—A European Journal

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована в березні 2012 (uk) im März 2012 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Daniel Canseco-Gonzalez et al published 29 March 2012 in Chemistry—A European Journal (en)
publication date	wds:Q57502919-65D19D3C-5A15-47E7-8D2D-92A530409AB9
publication date	2012-03-29 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57502919-D0EEC939-A78C-4CC1-8B87-9D7084F29F91
language of work or name	English
cites work	wds:Q57502919-0454FB35-7F61-4F18-87A7-E2D20AAF400C wds:Q57502919-051F3969-C3E0-4B78-91BA-F3500BBFDA37 wds:Q57502919-06BB934B-A5BA-4C09-AB6A-A15A9829A603 wds:Q57502919-0A79B0D0-CEC9-40D4-B9D8-3C57925211C2 wds:Q57502919-20000381-E33E-4909-B4D5-061157FDEF46 wds:Q57502919-202854EB-D7C5-4A6F-BD3C-BB58498BB024 wds:Q57502919-236E0174-0F23-4C73-B7E5-EC7510A455F4 wds:Q57502919-278EBB9F-5462-4B9B-A8E7-F43DA9A49DE3 wds:Q57502919-305CCB8B-EB6D-4894-94CD-E2551B8928B5 wds:Q57502919-35C87A50-428C-48A2-B17F-0B0B1B72FCB0 wds:Q57502919-36A4656C-6379-41D3-BA53-7E2CE7D0F509 wds:Q57502919-377127B1-7497-4AAC-9601-3D3FFA8B6FFB wds:Q57502919-39600EE7-2D08-4BC4-8584-AFDAA1765D0B wds:Q57502919-3DD7DB41-7A4C-456F-9BE0-6DEF80BFCCEE wds:Q57502919-49CA9E4E-3553-4DC9-BE1B-20C4BAA017DE wds:Q57502919-526EDC3B-810F-4060-ADAD-33B05F5703CE wds:Q57502919-5470A735-4E89-44F6-B66D-7B15DE832335 wds:Q57502919-577C2A63-16B0-4618-A2BE-CDADB1341528 wds:Q57502919-6255DB14-A4C7-4CCE-A490-C734734F58AE wds:Q57502919-6C751D93-10D6-4A01-883C-B1EB8BCC052F wds:Q57502919-6DB309E7-8884-486C-916C-1A745BB7C55A wds:Q57502919-7132F235-EEDC-4BE4-AF14-883F4F3D1A4E wds:Q57502919-71B4B260-E863-4913-A2C2-2381863E140A wds:Q57502919-7C65C12C-A18A-4261-8DA3-9B887D7AECF0 wds:Q57502919-7C77315C-D35B-4C14-8A55-F27640B90959 wds:Q57502919-81270133-D20B-4E75-89A1-57FF05D34D4E wds:Q57502919-84CEE8B3-ED87-447A-AB39-EB17F60586F5 wds:Q57502919-85A29755-C0D5-489F-A554-FA008BCED13B wds:Q57502919-86496E9B-00A5-4542-8493-64D345F3F13B wds:Q57502919-867202F8-1588-4C77-89FB-4314C07140B7 wds:Q57502919-87B5D180-9299-4FB1-9217-1EC79290B122 wds:Q57502919-8B63987D-1646-4D40-B711-DC5B59F0695F wds:Q57502919-91B8EA1E-6EF9-4590-8809-58CDAA342BAA wds:Q57502919-9306C5F9-2251-4A0E-9BBB-9CCF5FFA4928 wds:Q57502919-962CEC23-D7C8-4ED0-8785-B8712C7C6BA0 wds:Q57502919-9EDCD113-8219-4641-A62F-9421499F387E wds:Q57502919-A7EA75E0-A470-4481-BF56-1D41C0AAF48E wds:Q57502919-A928B837-1441-43B1-AC63-A04F9B6D3023 wds:Q57502919-AA853312-5AD8-4859-A68F-918E15C3CD1C wds:Q57502919-AB549A87-E99B-4099-BFAC-E0BF19942101 wds:Q57502919-ACDC6E29-8FD3-4C70-9EF1-78629F98EAFD wds:Q57502919-AD005330-440E-4C66-8F01-E5DC913D682C wds:Q57502919-C32817F3-D231-4DFE-AB1B-07C94D0FF8DE wds:Q57502919-CBDE794C-A5E2-4DFE-8A6D-908A3F1482B9 wds:Q57502919-CED44792-E402-45E6-BB41-76959FB0A5AE wds:Q57502919-D37D7994-20C9-4F39-A443-94F76AF71EAD wds:Q57502919-D40DC032-CA8D-436B-92A9-C4767A2A80AB wds:Q57502919-D8B8E766-5EC4-4EA4-8D65-A7C06BE68EB6 wds:Q57502919-E4B8C99D-01CA-4905-BB0C-601D59C29220 wds:Q57502919-F60E74E8-0D24-4934-9F50-20E84AF579AC wds:Q57502919-FCE2F083-77D6-4532-A608-F7766BE75BC9 wds:Q57502919-FDDC046A-0116-4345-AC89-8CC4C816818F
cites work	Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals New approach for size- and shape-controlled preparation of Pd nanoparticles with organic ligands. Synthesis and application in catalysis. A short history of SHELX 1,3-Dipolar Cycloadditions. Past and Future Carbon-heteroatom bond formation catalysed by organometallic complexes Cu-catalyzed azide-alkyne cycloaddition Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality Selected patented cross-coupling reaction technologies Tunable single-site ruthenium catalysts for efficient water oxidation Water Oxidation Catalyzed by Strong Carbene-Type Donor-Ligand Complexes of Iridium Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Cross-coupling reactions of organoboranes: an easy way to construct C-C bonds (Nobel Lecture). Palladium-catalyzed coupling reactions of aryl chlorides Mizoroki-Heck coupling using immobilized molecular precatalysts: leaching active species from Pd pincers, entrapped Pd salts, and Pd NHC complexes. The heck reaction as a sharpening stone of palladium catalysis Asymmetric transfer hydrogenation: chiral ligands and applications 1.3-Dipolare Cycloadditionen Rückschau und Ausblick A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst Beyond conventional N-heterocyclic carbenes: abnormal, remote, and other classes of NHC ligands with reduced heteroatom stabilization Mechanistic aspects of transition metal-catalyzed hydrogen transfer reactions. Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective Heterocyclic carbenes: synthesis and coordination chemistry. Structure-activity relationship analysis of Pd-PEPPSI complexes in cross-couplings: a close inspection of the catalytic cycle and the precatalyst activation model Stable cyclic carbenes and related species beyond diaminocarbenes A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides Rhodium-catalyzed methylenation of aldehydes Palladium nanoparticles as efficient green homogeneous and heterogeneous carbon-carbon coupling precatalysts: a unifying view Pyrazolin-4-ylidenes: a new class of intriguing ligands. Synthesis of Highly Stable 1,3-Diaryl-1H-1,2,3-triazol-5-ylidenes and their Applications in Ruthenium-Catalyzed Olefin Metathesis Crystalline 1H-1,2,3-triazol-5-ylidenes: new stable mesoionic carbenes (MICs). 1,2,3-Triazolylidenes as versatile abnormal carbene ligands for late transition metals Carbon−Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts Gold(i) “click” 1,2,3-triazolylidenes: synthesis, self-assembly and catalysis Seed-mediated synthesis of palladium nanorods and branched nanocrystals and their use as recyclable Suzuki coupling reaction catalysts. Protonolysis of a ruthenium-carbene bond and applications in olefin metathesis Oxidations and Oxidative Couplings Catalyzed by Triazolylidene Ruthenium Complexes

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