A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
about
A multiligand based Pd catalyst for C-N cross-coupling reactions.Pd-catalyzed amination as an alternative to nucleophilic aromatic substitution for the synthesis of N-alkyltacrines and analogues.Rational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis.Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts.Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design.Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions.Palladium-catalyzed amination of aryl chlorides and bromides with ammonium salts.Nickel-catalyzed amination of aryl chlorides with ammonia or ammonium saltsSlow reductive elimination from arylpalladium parent amido complexes.An examination of the palladium/Mor-DalPhos catalyst system in the context of selective ammonia monoarylation at room temperature.Promotion of selective pathways in isomerizing functionalization of plant oils by rigid framework substituents.Pd-Catalyzed Cyanation of (Hetero)Aryl Halides by Using Biphosphine Ligands.Pd-PEPPSI-IPent-SiO2 : A Supported Catalyst for Challenging Negishi Coupling Reactions in Flow.Solution structure of a pentachromium(ii) single molecule magnet from DFT calculations, isotopic labelling and multinuclear NMR spectroscopy.The synthesis of planar chiral pseudo-gem aminophosphine pre-ligands based on [2.2]paracyclophane.Solvent-free, microwave-assisted N-arylation of indolines by using low palladium catalyst loadings.D-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia.Synthesis of N-heterocyclic carbene-PdCl2-(iso)quinoline complexes and their application in arylamination at low catalyst loadings.Ni-Catalyzed Amination Reactions: An Overview.BippyPhos: a single ligand with unprecedented scope in the Buchwald-Hartwig amination of (hetero)aryl chlorides.
P2860
Q34369527-0306DCE7-AE0B-46A0-BBEB-0FFEAD05F348Q34535821-3D3DDCFD-59B5-43EF-B17E-F1A87A1108CCQ35233786-9DF11939-AFFE-4EAC-83F7-1EC10AE0791AQ37188811-90139E78-44F8-463A-8EF8-1AF9D4490DD8Q38025590-0E6676E2-DEFA-42BD-AE4B-E95A5AD96937Q38968855-0A5DB99F-1546-4A51-9CF5-F2467BC37C23Q42154147-F3881BBA-DCB4-48DA-BC94-1372785ED13CQ42406291-99AB96A3-6B6F-4920-9122-48422E728D67Q42425065-6CA0F752-6575-4BE0-9B76-082997482076Q46057405-CFFD3A69-D72C-42A2-BFE2-D3698DFD802FQ46825596-1376BC77-BD46-4639-A8EC-53DE1C075898Q48090377-352EB27D-5BD7-45C5-BDC8-068504D4FDA5Q48106267-B402DEBE-3E40-4AAA-8654-F3CFCE12588BQ49849172-674AE814-334C-40DA-86BF-75E989A69778Q50085909-197AD665-BD40-426A-A7EF-53E4D0558098Q50513320-180774D1-5B3B-4CCC-92FD-91B9555C8896Q50524327-FF5AC74F-E734-4A81-A467-BBF4886183E1Q51520918-0F533684-3E40-4BFB-90CC-65AEFB87AD01Q54302996-FAEDBD15-33FB-4BC9-A4E8-E10583AA9C76Q54528959-2DB00B0D-E342-42F3-BD41-C112D3E89E9E
P2860
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@en
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@nl
type
label
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@en
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@nl
prefLabel
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@en
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@nl
P356
P1476
A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines.
@en
P2093
Antonia Sappong-Kumankumah
Mark Stradiotto
P304
P356
10.1002/CHEM.200902316
P407
P577
2010-02-01T00:00:00Z