Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
about
Photoredox activation for the direct β-arylation of ketones and aldehydesPalladium-Catalyzed Ligand-Directed C−H Functionalization ReactionsWeak coordination as a powerful means for developing broadly useful C-H functionalization reactions.Auxiliary-assisted palladium-catalyzed arylation and alkylation of sp2 and sp3 carbon-hydrogen bonds.Pd(II)-catalyzed olefination of sp3 C-H bonds.Pd0/PR3-catalyzed arylation of nicotinic and isonicotinic acid derivativesAmide-Directed Arylation of sp C-H Bonds using Pd(II) and Pd(0) CatalystsDirect β-functionalization of cyclic ketones with aryl ketones via the merger of photoredox and organocatalysis.Cross-coupling of C(sp)-H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis**Pd(II)-catalyzed carbonylation of C(sp3)-H bonds: a new entry to 1,4-dicarbonyl compounds.Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes.Ligand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst.Pd(II)-Catalyzed Cross-Coupling of C(sp(2) )-H Bonds and Alkyl-, Aryl- and Vinyl-Boron Reagents via Pd(II)/Pd(0) CatalysisPd(II)-catalyzed C-H iodination using molecular I2 as the sole oxidant.Cross-coupling of remote meta-C-H bonds directed by a U-shaped template.Organopalladium(IV) chemistry.Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids.Transition metal-catalyzed arylation of unactivated C(sp3)-H bonds.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.Versatile reactivity of Pd-catalysts: mechanistic features of the mono-N-protected amino acid ligand and cesium-halide base in Pd-catalyzed C-H bond functionalization.Asymmetric palladium-catalyzed directed intermolecular fluoroarylation of styrenes.Heterocycle Formation via Palladium-Catalyzed C-H Functionalization.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.O-acetyl oximes as transformable directing groups for Pd-catalyzed C-H bond functionalization.Total synthesis and structural revision of the piperarborenines via sequential cyclobutane C-H arylation.N-Heterocyclic Carbene Ligand-Enabled C(sp(3))-H Arylation of Piperidine and Tetrahydropyran Derivatives.Palladium-Catalyzed Transformations of Alkyl C-H Bonds.β-C(sp(3))-H Arylation of α-Hydroxy Acid Derivatives Utilizing Amino Acid as a Directing Group.Ligand-Promoted Borylation of C(sp(3))-H Bonds with Palladium(II) Catalysts.Pd(II)-catalyzed C-H functionalizations directed by distal weakly coordinating functional groupsγ,δ,ε-C(sp(3))-H Functionalization through Directed Radical H-Abstraction.Ligand-enabled cross-coupling of C(sp(3))-H bonds with arylsilanes.Ligand-enabled β-C-H arylation of α-amino acids using a simple and practical auxiliary.Modifying electron transfer between photoredox and organocatalytic units via framework interpenetration for β-carbonyl functionalizationSingle operation palladium catalysed C(sp3)-H functionalisation of tertiary aldehydes: investigations into transient imine directing groupsPalladium-Catalyzed Directed C(sp(3))-H Arylation of Saturated Heterocycles at C-3 Using a Concise Optimization ApproachMechanistic comparison between Pd-catalyzed ligand-directed C-H chlorination and C-H acetoxylation.Aliphatic C-H to C-C conversion: synthesis of (-)-cameroonan-7α-ol.Selective Radical-Radical Cross-Couplings: Design of a Formal β-Mannich Reaction.Direct β-alkylation of aldehydes via photoredox organocatalysis.
P2860
Q24595336-083C54FF-3135-4C9D-8270-A37D2CCC315DQ29012891-C5C83003-66CC-4255-A694-4D38243D83C5Q30410596-8E1884CC-14E2-4570-9B40-9F594C2DD753Q33737426-59E67426-D7B2-4652-A08B-17CACED18882Q33738148-7EB4D79B-59A1-4EFE-A818-EE85EC25AA29Q33867816-8C03C862-D048-413E-A8CD-F9FA2024E10BQ34061734-020FAB4D-9345-4021-8B7B-1F59DD70FE84Q34385403-40608D2D-C339-4BD5-8AE2-46B2946BA55DQ34914538-1D084D9D-1771-4BA6-8B55-F8E29DF22AD0Q35103618-815AC334-A580-42E2-A0D9-FB34FDF99855Q35620535-DD0F6CF7-E837-4F70-AFEF-00F0CECEEBE3Q36405081-542CD476-73CF-428D-A030-0C2791DEFFD8Q36802674-1EEE4245-C2C2-4D79-B3B5-7F5F042768E6Q37146455-0040A6B5-7FE0-4D09-B394-FC151B50F6B2Q37372482-B4D8A501-1022-4279-AC19-53BD45D964FDQ37683501-ACB6A959-8657-4629-A833-007428B1845BQ37741356-D63865BA-E4D0-4208-BD81-9C95F5339961Q37867002-E80DA4BB-3ED7-4BEA-A896-C3C9AAAB04D5Q38097103-5D92D2E2-D939-4EC8-A9D8-4F899A1BB8F8Q38195732-EC9A836A-917A-4850-B096-508CB807D564Q38582683-C2AFC65C-47BF-416B-A1BF-76427539C44CQ38891800-015B4240-7723-4FB8-8BF4-E679A359A860Q39240715-36FB2CD4-22BF-43D5-A576-80F566312F1BQ39349576-99DF02FE-6C9A-46E9-9885-010259CDC406Q39361097-E53E329B-A88B-4FC3-9AC6-50DE04FC3CEEQ39424145-ED259FD1-D464-4F83-B1D1-10568AFFFA63Q39428953-3F1CE18E-592B-4AE4-AA53-D84D64AFF77EQ39780827-21A306ED-3382-4990-9FCE-9F629315EEEDQ39877406-9017B02F-52D3-478A-9C03-037351DD8326Q40657921-003A54CB-38DC-47C4-9913-553188999BF0Q40668223-AB752E19-C527-4B20-A528-76CA89759E75Q40700947-B966D375-F07F-42FE-A7A1-61776542670BQ40701143-B8EC9A71-0A12-4228-89E9-1F3D6B638268Q41527564-90049881-4864-4B23-87CD-806F7DFEE5C2Q41671104-39DF1D2F-E526-4E1B-972B-AEA95038DE0DQ41763219-F164B6FC-59E5-4DF5-B107-DBDAB2024FBEQ41832992-4B22F493-98BB-4787-A50C-69BD76402AD8Q41891161-45593594-9001-4236-8CFC-4929AD76386FQ41964947-4C4A698F-194A-429A-964C-D13813D609AEQ42091982-694A12E4-8E2F-4117-84C8-F9CD0BEB8F4C
P2860
Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
@en
type
label
Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
@en
prefLabel
Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
@en
P2860
P356
P1476
Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds
@en
P2093
Jin-Quan Yu
Masayuki Wasa
P2860
P304
P356
10.1021/JA903573P
P407
P577
2009-07-01T00:00:00Z