Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols. - Wikidata - wikimedia - TriplyDB

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

http://www.wikidata.org/entity/Q35166668

about

A bioinspired and biocompatible ortho-sulfiliminyl phenol synthesis.Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation.Scope and Mechanistic Study of the Coupling Reaction of α, β-Unsaturated Carbonyl Compounds with Alkenes: Uncovering Electronic Effects on Alkene Insertion vs Oxidative Coupling Pathways 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 carboxylation Ligand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst.Pd-catalyzed modifiable silanol-directed aromatic C-H oxygenation Pd(II)-catalyzed enantioselective C-H activation/C-O bond formation: synthesis of chiral benzofuranones.Pd(II)-catalyzed ortho- or meta-C-H olefination of phenol derivatives Ligand-Accelerated ortho-C-H Olefination of Phenylacetic Acids.Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst.Catalytic Reductive ortho-C-H Silylation of Phenols with Traceless, Versatile Acetal Directing Groups and Synthetic Applications of Dioxasilines C-H activation: a complementary tool in the total synthesis of complex natural products.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.Palladium-catalyzed cross-dehydrogenative functionalization of C(sp(2))-H Bonds.Arene C-H functionalisation using a removable/modifiable or a traceless directing group strategy.Asymmetric Synthesis of Chiral Atropisomeric Bis-Aryl Organophosphorus from Menthyl H-Phosphinate.Palladium catalysed meta-C-H functionalization reactions.Advances in the development of catalytic tethering directing groups for C-H functionalization reactions.Ligand-accelerated cross-coupling of C(sp2)-H bonds with arylboron reagents.Pd(II)-catalyzed C-H functionalizations directed by distal weakly coordinating functional groups Copper-catalyzed recycling of halogen activating groups via 1,3-halogen migration.Meta-selective C-H functionalization using a nitrile-based directing group and cleavable Si-tether.Stereoselective synthesis of silicon-stereogenic aminomethoxysilanes: easy access to highly enantiomerically enriched siloxanes.Palladium-catalyzed ortho-alkenylation of aryl hydrogen phosphates using a new mono-phosphoric acid directing group.Ruthenium(II)-catalyzed C-H alkenylations of phenols with removable directing groups.Rh-catalyzed sulfonic acid group directed ortho C-H olefination of arenes.Ligand-accelerated non-directed C-H functionalization of arenes.Controllable Mono-/Dialkenylation of Benzyl Thioethers through Rh-Catalyzed Aryl C-H Activation.Towards ideal synthesis: alkenylation of aryl C-H bonds by a Fujiwara-Moritani reaction.Versatile palladium-catalyzed C-H olefination of (hetero)arenes at room temperature.Chelation versus Non-Chelation Control in the Stereoselective Alkenyl sp2 C-H Bond Functionalization Reaction.Silicon-Tethered Strategies for C-H Functionalization Reactions.A meta-selective-C-H alkenylation of phenol-derivatives employing a traceless organosilicon template.A bentonite-gold nanohybrid as a heterogeneous green catalyst for selective oxidation of silanes.2-Pyridylmethyl ether: a readily removable and efficient directing group for amino acid ligand accelerated ortho-C-H olefination of phenols.Rhodium(iii)-catalyzed and MeOH-involved regioselective mono-alkenylation of N-arylureas with acrylates.Oxidative Mizoroki-Heck-type reaction of arylsulfonyl hydrazides for a highly regio- and stereoselective synthesis of polysubstituted alkenes.Palladium-Catalyzed Directed para C-H Functionalization of Phenols.Reductive arene ortho-silanolization of aromatic esters with hydridosilyl acetals.

P2860

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P2860

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

http://www.wikidata.org/entity/Q35166668

description

2011 nî lūn-bûn

@nan

2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@ast

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@en

type

label

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@ast

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@en

prefLabel

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@ast

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@en

P1433

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P356

P1433

Journal of the American Chemical Society

P1476

Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols.

@en

P2093

Buddhadeb Chattopadhyay

http://www.w3.org/2001/XMLSchema#string

Chunhui Huang

http://www.w3.org/2001/XMLSchema#string

Vladimir Gevorgyan

http://www.w3.org/2001/XMLSchema#string

P2860

Thyroid receptor ligands. 6. A high affinity "direct antagonist" selective for the thyroid hormone receptor

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

Ligand-enabled reactivity and selectivity in a synthetically versatile aryl C-H olefination

Pd(II)-catalyzed enantioselective C-H olefination of diphenylacetic acids

Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.

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.

Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage.

Claisen rearrangement over the past nine decades.

Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.

P304

12406-12409

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P31

scholarly article

P356

10.1021/JA204924J

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P433

32

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P478

133

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P577

2011-07-21T00:00:00Z

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51499975

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P698

21766826

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P932

3156791

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