Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.
about
Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable MethodC-H bond halogenation catalyzed or mediated by copper: an overviewSpacer-free BODIPY fluorogens in antimicrobial peptides for direct imaging of fungal infection in human tissueRadicals: Reactive Intermediates with Translational PotentialPalladium-catalysed transannular C-H functionalization of alicyclic aminesPalladium-Catalyzed Ligand-Directed C−H Functionalization ReactionsDecarbonylative organoboron cross-coupling of esters by nickel catalysis.Catalytic ch bond addition of pyridines to allenes by a rare-Earth catalyst.Non-redox metal ions can promote Wacker-type oxidations even better than copper(II): a new opportunity in catalyst design.[N,P]-pyrrole PdCl2 complexes catalyzed the formation of dibenzo-α-pyrone and lactam analogues.C-H Bond Activation/Arylation Catalyzed by Arene-Ruthenium-Aniline Complexes in Water.Palladium-catalyzed regioselective azidation of allylic C-H bonds under atmospheric pressure of dioxygen.Sonogashira diversification of unprotected halotryptophans, halotryptophan containing tripeptides; and generation of a new to nature bromo-natural product and its diversification in water.Chemical and biological studies of nakiterpiosin and nakiterpiosinone.C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition.Peptide-templated noble metal catalysts: syntheses and applicationsControllable cyanation of carbon-hydrogen bonds by zeolite crystals over manganese oxide catalyst.Auxiliary-assisted palladium-catalyzed arylation and alkylation of sp2 and sp3 carbon-hydrogen bonds.Pd(II)-catalyzed olefination of sp3 C-H bonds.The total synthesis of K-252c (staurosporinone) via a sequential C-H functionalisation strategy.Pd0/PR3-catalyzed arylation of nicotinic and isonicotinic acid derivativesFormation of a C-C double bond from two aliphatic carbons. Multiple C-H activations in an iridium pincer complex.Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands.PyDipSi: a general and easily modifiable/traceless Si-tethered directing group for C-H acyloxylation of arenes.Amide-Directed Arylation of sp C-H Bonds using Pd(II) and Pd(0) CatalystsCationic Pd(II)-catalyzed Fujiwara-Moritani reactions at room temperature in water.On the mechanism of palladium-catalyzed aromatic C-H oxidationExploring bis(cyclometalated) ruthenium(II) complexes as active catalyst precursors: room-temperature alkene-alkyne coupling for 1,3-diene synthesis.Palladium(III) in Synthesis and Catalysis.Regioselective oxidative arylation of indoles bearing N-alkyl protecting groups: dual C-H functionalization via a concerted metalation-deprotonation mechanism.Natural product synthesis at the interface of chemistry and biology.Total synthesis of (+)-linoxepin by utilizing the Catellani reaction.General method for functionalized polyaryl synthesis via aryne intermediates.Room-Temperature Direct β-Arylation of Thiophenes and Benzo[b]thiophenes and Kinetic Evidence for a Heck-type PathwayDirected Evolution of RebH for Catalyst-Controlled Halogenation of Indole C-H BondsRh(III)-catalyzed oxidative coupling of unactivated alkenes via C-H activation.Chelate-Assisted Oxidative Coupling Reaction of Arylamides and Unactivated Alkenes: Mechanistic Evidence for Vinyl C-H Bond Activation Promoted by an Electrophilic Ruthenium-Hydride CatalystRhodium(III)-catalyzed arylation of Boc-imines via C-H bond functionalization.Base-mediated intermolecular sp2 C-H bond arylation via benzyne intermediates.Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reaction
P2860
Q26747345-B20B51D8-2FC9-4640-9672-8D6B7612058AQ26776189-AA3DA873-24A9-4450-A0BB-966438D29574Q27324625-CD233E7D-88E2-4A98-A1DD-6847A913B5DFQ28468198-795EE8C2-ECA3-4CC4-9D10-42F48AACA218Q28820908-0CB68A32-BDF1-452E-9327-6F94DA1B9E88Q29012891-328BC316-B7C1-4AFD-BC2C-4AC471D22377Q30656755-ED43C97F-2731-4B3C-8599-71A6739537C9Q30938323-B26E74FA-4984-4327-9C1A-00159EA111FFQ30995038-352FFF16-7497-46A5-9156-981FAB4DB837Q31101298-6AE06983-5AA6-4EBE-9357-E4F4C0DC7ECFQ31122924-0B571A31-5C21-45DF-ADBF-E3862486DB6BQ33461327-E35773B6-B20C-4D8B-8A7A-D62738F31D26Q33583746-6725BDA9-2CE5-4264-B3EB-CF0D37629FDDQ33584817-A3CF7F79-8B48-4BAA-9039-0928887BFEBBQ33626822-7419781B-A602-4F1E-8D42-A7604B2838D4Q33636198-C6627A48-4E5A-4BD0-A798-253BA1D5C2F4Q33715922-3F99A2BA-51F9-44DC-94F6-0F3298834466Q33737426-45330893-F12C-4536-8691-C8E46A768A4BQ33738148-EB8B4D04-9FC8-4C23-A69E-F9387F273B51Q33814105-432E05BE-DFD8-4438-8364-F098AA59BA3CQ33867816-331C0769-FAD7-4FF8-9AFF-F1DB1585A064Q33869691-B033DEB8-B44C-4E8E-A9C2-6E3487AE426BQ33899813-0C211521-2029-4717-B8E1-6CAF2A4A57A0Q33940348-B10E895D-A0D6-46C7-BF0E-4A27383732BDQ34061734-9B35907B-C2C4-4ABD-A541-A35986DC938DQ34108251-B6A69F89-5598-445C-831F-4B6ECAD16570Q34140301-80B061D8-DA24-4DDA-9F5C-30EAE0E3E316Q34146299-33B5BBBF-9E8B-484F-8BC2-EFAACB012402Q34175475-82F74E64-A721-4A47-831B-C309B4921369Q34195420-A29D8C37-141D-4DA4-88A2-13214AF18D2FQ34202358-0EBA4636-4555-4879-8D70-B208F60D5467Q34339731-2A404784-673A-48BE-918C-4C3A9D992492Q34489853-EF9727CE-A0FD-46E9-A246-3077E184E47BQ34509995-36FFE9EA-8B89-4771-9237-B189DDB08249Q34532086-513F761D-FA18-4CC3-98C7-E44A984E1901Q34543120-9808052F-0F4E-4D0D-83E9-4CE8FD6575F3Q34587261-CC395A42-2C31-4CA5-B3F4-8C176E1B31C7Q34608941-AC4C9211-EE94-4E58-9BE8-AA31AF91B417Q34731126-934F9E37-CF24-4DE5-A1F6-7E19D94BA8B0Q34751859-7DB4BF0B-36B1-43C8-A3F0-B4BF15F6C2CA
P2860
Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Palladium(II)-catalyzed C-H ac ...... versatility and practicality.
@en
type
label
Palladium(II)-catalyzed C-H ac ...... versatility and practicality.
@en
prefLabel
Palladium(II)-catalyzed C-H ac ...... versatility and practicality.
@en
P2860
P356
P1476
Palladium(II)-catalyzed C-H ac ...... versatility and practicality.
@en
P2093
Jin-Quan Yu
P2860
P304
P356
10.1002/ANIE.200806273
P407
P577
2009-01-01T00:00:00Z