about
Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalyst.Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds.Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.Double-fold C-H oxygenation of arenes using PyrDipSi: a general and efficient traceless/modifiable silicon-tethered directing group.General method for the synthesis of salicylic acids from phenols through palladium-catalyzed silanol-directed C-H carboxylationPd-catalyzed modifiable silanol-directed aromatic C-H oxygenationGeneral and practical carboxyl-group-directed remote C-H oxygenation reactions of arenes.Purinyl N1-directed aromatic C-H oxidation in 6-arylpurines and 6-arylpurine nucleosides.Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design.Efficient palladium-catalyzed cross-coupling of highly acidic substrates, nitroacetates.Synthesis of aryl ethers from benzoates through carboxylate-directed C-H-activating alkoxylation with concomitant protodecarboxylation.Copper-catalyzed dehydrogenative coupling of arenes with alcohols.Broadening the catalyst and reaction scope of regio- and chemoselective C-H oxygenation: a convenient and scalable approach to 2-acylphenols by intriguing Rh(II) and Ru(II) catalysis.Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad.Rh(V) -Nitrenoid as a Key Intermediate in Rh(III) -Catalyzed Heterocyclization by C-H Activation: A Computational Perspective on the Cycloaddition of Benzamide and Diazo Compounds.Phosphane-functionalized cycloheptatrienyl-cyclopentadienyl titanium sandwich complexes: phosphorus ligands with an integrated reducing agent for palladium(0) catalyst generation.Synthesis of Complex Phenols Enabled by a Rationally Designed Hydroxide Surrogate.An iron-catalyzed hydroalkylation reaction of α,β-unsaturated ketones with ethers.Synthesis of 2,2'-biphenols through direct C(sp(2))-H hydroxylation of [1,1'-biphenyl]-2-ols.Continuous-flow synthesis of functionalized phenols by aerobic oxidation of Grignard reagents.Palladium catalyzed Csp2-H activation for direct aryl hydroxylation: the unprecedented role of 1,4-dioxane as a source of hydroxyl radicals.Copper-catalyzed aromatic C-H alkoxylation with alcohols under aerobic conditions.Enhancement of neighbouring-group participation in Cu0-promoted cross-coupling gem-difluoromethylenation of aryl/alkenyl halides with 1,3-azolic difluoromethyl bromides.Redox inactive metal ion promoted C-H activation of benzene to phenol with Pd(II)(bpym): demonstrating new strategies in catalyst designs.Cobalt-catalyzed C(sp(2))-H alkoxylation of aromatic and olefinic carboxamides.Ether formation through reductive coupling of ketones or aldehydes catalyzed by a mesoionic carbene iridium complexPalladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp2 C–H bond activationCobalt-catalyzed -selective alkoxylation of 1-naphthylamine derivatives
P2860
Q33725567-21329AA1-24E1-46CD-AEC6-5D76872D78F6Q33833213-2E0B1BFA-2E87-46AD-A865-FACE69A803E8Q35648469-0A980657-B28F-4694-8BEA-25EE4D0A50B3Q36021897-304718ED-0AB5-4D6F-9736-CFAA57EBC183Q36047548-5AC80D3D-783A-46F1-ABFC-252152173019Q36452868-6666319B-4D02-4B17-A3DE-04F7057AB019Q37374955-14B50803-E63D-4D51-A857-CD56B662D385Q37673934-B63E25D7-1839-4494-8872-1189FC4DAA6DQ38025590-05D58087-5780-4953-8C12-311E32C7ACD9Q42230728-62754628-EC8A-4B0B-A131-35BA17809C3AQ43698555-5B32231A-9E91-46EC-8AB9-EB0C561B5816Q45206680-0C44122D-C6A9-40B1-96FA-50A062F665C3Q46026417-B660BEB0-C5A5-40EB-9EF8-9A9B57FFD63EQ46601949-E2C51EF0-9198-4667-BA5A-5684B3797C08Q46727591-1D742828-4551-46F1-B781-4B107E3E9F36Q46800384-0AD9C121-88C3-46CB-ABAE-F5A251A57B8BQ48366114-065ECDBD-D1DC-4DF5-8396-D14A72AD388BQ48612631-509287FC-C333-4F08-8686-A1C775B18F4EQ50222298-20EF0DFA-780C-4C19-A43F-D176B44B0C29Q50460940-1272AC29-43C9-4AF1-BC62-F1B8251746D2Q51036062-6E65139C-6216-4BF4-91EE-6E58328CAD72Q51039635-3220E39B-606E-4ED0-AA9E-7C2123EDA506Q51070416-8E72DFA1-B8F6-4233-80A8-D67E2AB9AFB7Q51831815-CA2F972A-E696-48DA-AD2D-37761F182072Q53392746-00C05510-7C1F-4CF3-A95B-388D0AEBF366Q57502835-2B6FF299-BB29-41D9-949A-BBB36B66427DQ57614533-5B3C06F9-FD84-4FFB-8A33-3574749CE107Q58792406-96195E7A-B101-41E0-8B11-3AF11CF918FF
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 06 June 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Palladium-catalysed hydroxylation and alkoxylation.
@en
Palladium-catalysed hydroxylation and alkoxylation.
@nl
type
label
Palladium-catalysed hydroxylation and alkoxylation.
@en
Palladium-catalysed hydroxylation and alkoxylation.
@nl
prefLabel
Palladium-catalysed hydroxylation and alkoxylation.
@en
Palladium-catalysed hydroxylation and alkoxylation.
@nl
P2860
P356
P1476
Palladium-catalysed hydroxylation and alkoxylation.
@en
P2860
P304
P356
10.1039/C1CS15085E
P577
2011-06-06T00:00:00Z