About: Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on December 2006

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2006 (ast) наукова стаття, опублікована в грудні 2006 (uk) مقالة علمية نشرت في ديسمبر 2006 (ar) scientific article published on December 2006 (en)
publication date	wds:Q37014864-F813072D-D7C4-4CAE-87CC-EDD66E1C02F3
publication date	2006-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37014864-D49ADC66-D824-4F28-AB21-7843A3E879C3
language of work or name	English
cites work	wds:Q37014864-064B6416-BE30-45B9-8F69-A64AA51BAF6B wds:Q37014864-0C81F0CB-A143-464D-8491-BDEA23A65F13 wds:Q37014864-0D827CFD-D040-4EBB-BFD1-E8ED6D478E90 wds:Q37014864-154BFA84-C02C-495D-9EB6-F70CAB6EAD19 wds:Q37014864-16615347-7192-4FD8-A696-655113CAC240 wds:Q37014864-1CE4934F-450F-4D7D-B576-3659B586780F wds:Q37014864-24938A8B-BAD2-4CA3-ACA1-CE91F19D522B wds:Q37014864-2BD94974-2AA3-4AA7-B28D-8BD79030550D wds:Q37014864-2EEFB21F-DB5D-4C17-9C85-18953F7340A3 wds:Q37014864-31BEE87E-4786-4292-8C7E-35CB6D41F024 wds:Q37014864-31F1D34C-0451-493B-91DD-6A194418E615 wds:Q37014864-43DAFA2F-2916-4669-B46F-DC6F62D03E72 wds:Q37014864-730C1809-A8AE-4DAC-9C68-607C324DDB74 wds:Q37014864-886C1FD7-06D8-4981-B47B-9F9389B76E7B wds:Q37014864-8B7FDC91-F024-4FBD-91A2-15C99A91E415 wds:Q37014864-9CF8EF76-B47E-435F-9A3A-F8BFB7F75D7C wds:Q37014864-9E8EF89C-01B2-46F3-8171-790EC7A5FC87 wds:Q37014864-A01CFCE5-8B37-458A-880D-5B49FD1AA543 wds:Q37014864-A9431F19-8EBD-423F-9797-29F7F4A6D9B1 wds:Q37014864-B2409AC0-5764-42D4-ACDF-FBC36C485D01 wds:Q37014864-BE663975-30BF-48BC-94A4-4F95AD62BDA7 wds:Q37014864-D614637F-ADE1-4268-8C9A-2FF71135C568 wds:Q37014864-E5BAE331-0775-4813-B5A2-C6B169314C57 wds:Q37014864-E8876EDF-F10A-4E3C-A3C8-936ABC5DD25D
cites work	The first ligand-modulated oxidative Heck vinylation. Efficient catalysis with molecular oxygen as palladium(0) oxidant Expanding organoboron chemistry: epoxidation of potassium organotrifluoroborates Mechanism of the Palladium-Catalyzed Homocoupling of Arylboronic Acids: Key Involvement of a Palladium Peroxo Complex The heck reaction as a sharpening stone of palladium catalysis Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins Mizoroki-Heck type reaction of organoboron reagents with alkenes and alkynes. A Pd(II)-catalyzed pathway with Cu(OAc)2 as an oxidant Mild and efficient aryl-alkenyl coupling via Pd(II) catalysis in the presence of oxygen or Cu(II) oxidants Vinylic tellurides: from preparation to their applicability in organic synthesis. Preparation of enamides via palladium-catalyzed amidation of enol tosylates A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions Palladium oxidase catalysis: selective oxidation of organic chemicals by direct dioxygen-coupled turnover Screening of homogeneous catalysts by fluorescence resonance energy transfer. Identification of catalysts for room-temperature Heck reactions. Toward waste-free production of Heck products with a catalytic palladium system under oxygen Oxidative addition of aryl tosylates to palladium(0) and coupling of unactivated aryl tosylates at room temperature The palladium-catalyzed oxidative kinetic resolution of secondary alcohols with molecular oxygen Green, catalytic oxidation of alcohols in water Oxygenation of nitrogen-coordinated palladium(0): synthetic, structural, and mechanistic studies and implications for aerobic oxidation catalysis Palladium-catalyzed enantioselective oxidations of alcohols using molecular oxygen Synthetic applications of o- and p-halobenzyl sulfones as zwitterionic synthons: preparation of ortho-substituted cinnamates and biarylacetic acids Electronic control of the regiochemistry in the Heck reaction Mechanistic study of alcohol oxidation by the Pd(OAc)(2)/O(2)/DMSO catalyst system and implications for the development of improved aerobic oxidation catalysts Regioselective Heck couplings of alpha,beta-unsaturated tosylates and mesylates with electron-rich olefins Highly regioselective palladium-catalyzed beta-arylation of N, N-dialkylallylamines Oxygen-promoted palladium(II) catalysis: facile C(sp2)-C(sp2) bond formation via cross-coupling of alkenylboronic compounds and olefins
author name string	wds:Q37014864-3B53E626-C88B-4848-AB1F-A139BB6CC138 wds:Q37014864-54B3A4DF-919A-48DB-95CC-34E90418F66E wds:Q37014864-785D368C-51C0-452E-ABC5-370D201F35A7 wds:Q37014864-8A85B740-13BA-425D-8B54-12B723AF39F9 wds:Q37014864-C779FC9D-6EC4-473B-88A8-EDE460EC4028 wds:Q37014864-C902306D-753E-4B03-9B7F-A873418E6ED4
author name string	Rajesh K Mishra Sung Wook Yi Kyung Soo Yoo Kyung Woon Jung Cheol Hwan Yoon Young Chun Jung
rdfs:label	Oxidative palladium (nl) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (en) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (ast)
skos:prefLabel	Oxidative palladium (nl) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (en) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (ast)
name	Oxidative palladium (nl) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (en) Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (ast)
title	wds:Q37014864-530471D7-8C2B-4580-980A-8C26E6EF10E0
title	Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (en)
page(s)	wds:Q37014864-78969A8E-635D-4F84-8757-43C6536EEB8F
page(s)	16384-16393
instance of	wds:Q37014864-6CA4FBBF-4DA6-4356-ACE4-2A7FB48C2E50
instance of	scholarly article
main subject	wds:Q37014864-687EC624-363E-4DF6-84B8-88D4550990CC
main subject	palladium
PubMed ID	wds:Q37014864-FE7A44E1-881A-4D7E-8301-D04C048539C5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17165795

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software