About: Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins

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About: Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 2003

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2003 (uk) im Juni 2003 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 2003 (ast) scientific article published on 01 June 2003 (en)
publication date	wds:Q73551647-F3E5AF25-E318-4DB0-86D8-7F53A80DF61E
publication date	2003-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73551647-3C68054B-D344-4F7C-A9FD-344A7424E237 wds:Q73551647-595AF8DC-BAF7-488A-8894-5E37B2D27A92 wds:Q73551647-7C547AC9-1896-423F-9824-FC9591B6A33D wds:Q73551647-F35B53E6-B392-4D00-AF96-DCC2D9D2476D
author name string	Kyung Woon Jung Rajesh Kumar Mishra Cheol Hwan Yoon Young Chun Jung
rdfs:label	Oxygen-promoted Pd (nl) Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins (en)
skos:prefLabel	Oxygen-promoted Pd (nl) Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins (en)
name	Oxygen-promoted Pd (nl) Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins (en)
title	wds:Q73551647-59029762-14A0-418F-8443-B039EFA4BB1A
title	Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins (en)
page(s)	wds:Q73551647-FA741887-DF4F-486F-9693-179B1BDBA576
page(s)	2231-2234
instance of	wds:Q73551647-80EFCF5B-9C23-4E7A-8439-2FC37A0504D2
instance of	scholarly article
PubMed ID	wds:Q73551647-1D2FE450-7ADC-4E08-87E9-DAACDB3514B5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12816416
PubMed ID	12816416
published in	wds:Q73551647-7218430E-5E51-471E-BFFA-C0E847707045
published in	Organic Letters
issue	wds:Q73551647-50CE9103-F989-4D9D-9E30-584C0089FF2D
volume	wds:Q73551647-C4671E3F-1D82-4FAE-96FF-622175AA62AD
issue	13
volume	5
DOI	wds:Q73551647-40892128-A925-4D51-91AE-D7076E1A52D7
DOI	http://dx.doi.org/10.1021/OL034458S
DOI	10.1021/OL034458S
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73551647
is cites work of	A highly selective and general palladium catalyst for the oxidative Heck reaction of electronically nonbiased olefins Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions Palladium-catalyzed oxidative intermolecular difunctionalization of terminal alkenes with organostannanes and molecular oxygen Oxidative Heck vinylation for the synthesis of complex dienes and polyenes Recent advancements and challenges of palladium(II)-catalyzed oxidation reactions with molecular oxygen as the sole oxidant Palladium-Catalyzed 1,3-Difunctionalization Using Terminal Alkenes with Alkenyl Nonaflates and Aryl Boronic Acids Pd(II)-catalyzed oxidative 1,1-diarylation of terminal olefins Enantioselective redox-relay oxidative heck arylations of acyclic alkenyl alcohols using boronic acids Transmetallation versus β-hydride elimination: the role of 1,4-benzoquinone in chelation-controlled arylation reactions with arylboronic acids Enantioselective Fujiwara-Moritani Indole and Pyrrole Annulations Catalyzed by Chiral Palladium(II)-NicOx Complexes Regioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: efficient access to α-alkyl vinylarenes. Operationally simple and highly (E)-styrenyl-selective Heck reactions of electronically nonbiased olefins Catalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions. The Suzuki homocoupling reaction under high-intensity ultrasound Chemoselective Three-Component Coupling via A Tandem Pd Catalyzed Boron-Heck and Suzuki Reaction Asymmetric intermolecular boron Heck-type reactions via oxidative palladium(II) catalysis with chiral tridentate NHC-amidate-alkoxide ligands Pd(OAc)2/p-Benzoquinone-Catalyzed Anaerobic Electrooxidative Homocoupling of Arylboronic Acids, Arylboronates and Aryltrifluoroborates in DMF and/or Water Oxidative Heck Reactions using Aryltrifluoroborates and Aryl N-Methyliminodiacetic Acid (MIDA) Boronates Development and Investigation of a Site Selective Palladium-Catalyzed 1,4-Difunctionalization of Isoprene using Pyridine-Oxazoline Ligands C–C Coupling Reaction of Triphenylbismuth(V) Derivatives and Olefins in the Presence of Palladium Nanoparticles Immobilized in Spherical Polyelectrolyte Brushes
is cites work of	wds:Q33750247-993E0CEA-F8FD-41A5-87A8-7ECEA31915BE wds:Q37005564-5BA180DA-EA90-43BE-8BEA-05E154B54514 wds:Q42723150-ECD5B73E-4BC3-4FFE-B166-BD125AA8E822 wds:Q57391642-FA808633-5043-428B-BF7C-05E630EC1442 wds:Q33560690-5ABD9262-ECA4-46EF-BA52-E04D75CD58AA wds:Q34178015-8E1D2F8C-9134-44FB-8F4E-536C8852B4BD wds:Q35097896-08D21E07-554D-45A7-ADFC-C022C76CC04F wds:Q40665487-15EF8B32-2F17-47F7-976B-47DAD423525A wds:Q59203498-D35D63C0-9A72-4A52-B410-CCBE929113B4 wds:Q34446745-03D739DB-23F7-49B5-BC75-C427027814E4 wds:Q38856166-8616BB63-DCCE-4B84-B916-74E1D99EA3D8 wds:Q37316120-C535E865-E04E-447A-9748-C78A4B3DDDA3 wds:Q42128736-2D580F7B-5D99-4D79-805C-4D5A21E69732 wds:Q36974478-CA321220-BA27-461C-BF33-9690E569A359 wds:Q37014864-43DAFA2F-2916-4669-B46F-DC6F62D03E72 wds:Q35070577-6A385BBA-EB33-46AD-928A-A3002038BF55 wds:Q35100458-BD945733-F320-48D5-8069-67591851CCA5 wds:Q64174714-77B0F6BF-7DC2-4AA8-868C-5CAC8DFFDD15 wds:Q34015488-3DBDB1CC-DF32-4480-81B3-C9FBB759487F wds:Q36392607-C9EF5D16-5F43-46F2-A427-A6530DA1A0E0 wds:Q45098927-4E300642-C8B5-4EF6-9C68-2F2C30818936

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