About: Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones

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scientific article published on 10 January 2011

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) bài báo khoa học (vi) наукова стаття, опублікована в січні 2011 (uk) article scientifique publié en 2011 (fr) scientific article published on 10 January 2011 (en) 2011 թվականի հունվարի 10-ին հրատարակված գիտական հոդված (hy) artículu científicu espublizáu en xineru de 2011 (ast)
publication date	wds:Q83157752-35EBB609-3F4F-41D0-9A40-7F0A4242BD9F
publication date	2011-01-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q83157752-C0522B52-5E1F-4615-8968-C0D0099C170A
language of work or name	English
author name string	wds:Q83157752-005A82BA-0460-423F-B385-AFFF74DFB300 wds:Q83157752-8061FF4F-FB59-40F5-B838-6B64018525CE wds:Q83157752-8511B2A4-F167-47CA-BB5E-9904C461A7BE wds:Q83157752-F46BFDD6-8083-49B6-A294-3A768A5924E8
author name string	Jun Xu Lei Liu Zhao-Jing Liu Tian-Jun Gong
rdfs:label	Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (en) Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (nl)
skos:prefLabel	Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (en) Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (nl)
name	Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (en) Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (nl)
author	wds:Q83157752-29832757-5787-4EBF-8D88-F5BE460322BF
author	Bin Xiao
title	wds:Q83157752-7E0B6EAA-F05E-46DA-AEC6-642D7031EB21
title	Palladium-catalyzed intermolecular directed C-H amidation of aromatic ketones (en)
page(s)	wds:Q83157752-7AD288F0-1E08-4E4D-A958-4B8450295FE2
page(s)	1466-1474
instance of	wds:Q83157752-D775441A-042C-4814-89E1-EB3756C50564
instance of	scholarly article
PubMed ID	wds:Q83157752-793E1F59-6842-4D46-951C-5CE82F694397
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21218796
PubMed ID	21218796
published in	wds:Q83157752-DD8AC86D-6A80-45FF-8081-EF1F5904B08A
published in	Journal of the American Chemical Society
issue	wds:Q83157752-CD6519ED-42FA-4002-AA04-C55D3B31FD8F
volume	wds:Q83157752-427FCE03-6867-472F-AB66-9086B2688A7B
issue	5
volume	133
DOI	wds:Q83157752-06DD10A1-4958-4A6A-AFBC-8D3183FA7102
DOI	http://dx.doi.org/10.1021/JA108450M
DOI	10.1021/JA108450M
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q83157752
is cites work of	Copper-catalyzed electrophilic amination of heteroarenes and arenes by C-H zincation Directed amination of non-acidic arene C-H bonds by a copper-silver catalytic system Metal-free intermolecular oxidative C-N bond formation via tandem C-H and N-H bond functionalization Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst N-Acyloxyphthalimides as nitrogen radical precursors in the visible light photocatalyzed room temperature C-H amination of arenes and heteroarenes A General Method for Aminoquinoline-Directed, Copper-Catalyzed sp(2) C-H Bond Amination Pd-catalyzed aryl C-H imidation with arene as the limiting reagent Identification of monodentate oxazoline as a ligand for copper-promoted ortho-C-H hydroxylation and amination A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols. Pd(II)-catalyzed C-H functionalizations directed by distal weakly coordinating functional groups Regioselective C-H bond amination by aminoiodanes Ruthenium-Catalyzed C-H Arylation of Benzoic Acids and Indole Carboxylic Acids with Aryl Halides Intermolecular Aryl C-H Amination through Sequential Iron and Copper Catalysis. Palladium(0)-catalyzed intermolecular amination of unactivated C(sp³)-H bonds Palladium-Catalyzed Synthesis of Aromatic Sultones via Sulfonic Acid Group-Directed CH Activation Radical-mediated direct C–H amination of arenes with secondary amines Copper-Catalyzed Redox Coupling of Nitroarenes with Sodium Sulfinates Ligand-Enabled, Palladium-Catalyzed β-C(sp3)-H Arylation of Weinreb Amides Cationic Pd(II)-catalyzed C-H activation/cross-coupling reactions at room temperature: synthetic and mechanistic studies Aromatic C-H addition of ketones to imines enabled by manganese catalysis Site-Selective Copper-Catalyzed Amination and Azidation of Arenes and Heteroarenes via Deprotonative Zincation. Palladium Catalyzed Aryl C-H Amination with O2 via In Situ Formation of Peroxide-Based Oxidant(s) from Dioxane An Efficient, One-Pot Transamidation of 8-Aminoquinoline Amides Activated by Tertiary-Butyloxycarbonyl Synthesis of Indole-2-carboxylate Derivatives via Palladium-Catalyzed Aerobic Amination of Aryl C-H Bonds Recent Advances in the Application of Selectfluor™ F-TEDA-BF4 as a Versatile Mediator or Catalyst in Organic Synthesis. N-Aminopyridinium Ylide-Directed, Copper-Promoted Amination of sp2 C-H Bonds Relative Strength of Common Directing Groups in Palladium-Catalyzed Aromatic C-H Activation Electrooxidative para-selective C-H/N-H cross-coupling with hydrogen evolution to synthesize triarylamine derivatives A diversity-oriented synthesis of bioactive benzanilides via a regioselective C(sp2)-H hydroxylation strategy.
is cites work of	wds:Q37206766-95F0C5E0-942F-4344-B53B-0A278F46410F wds:Q42126723-F4C28BA4-6466-4835-82DE-EB8C5D466AD5 wds:Q57614613-737CFB17-13E1-4D80-BBB4-A70BD504AF5B wds:Q64060516-22AB1116-C682-43DF-A23F-B4B51E56328D wds:Q36145643-B5975A35-6E02-48C5-B650-A43AFDF17BDC wds:Q42157831-576F7776-BB97-4A45-8083-EA9537F4043C wds:Q42611738-64407F5B-0930-46B2-8150-FF9195D00517 wds:Q33625981-F8BD407B-EFB1-4886-9711-D469E53E4A47 wds:Q40657921-E1801036-7000-4C67-96D8-1473914F270C wds:Q48329923-3850FC53-2F29-40EA-94DE-7A74DD3A9ED8 wds:Q41889192-C4E7C472-A7AA-48BD-BFE1-0E71246FD4A1 wds:Q42921433-7037C64A-4E68-4D77-BD7E-6058BC8A4C4A wds:Q39046016-96189B52-1198-4E53-A7A4-409C369DDED9 wds:Q42133005-3217D31B-3751-446D-8D34-3115F8910563 wds:Q42734645-392E7F21-3FFE-435A-AAD6-DCB2F16A189D wds:Q55154908-04FE968F-31F2-4590-9C5C-8EE43C2320A1 wds:Q90015611-0E5686AD-9C2E-4621-8B04-8A67C93653F9 wds:Q90719429-E28151F3-2933-4245-8518-EBB47907FB74 wds:Q92929923-95473B81-C1BA-4C88-9126-3D93E36EECD6 wds:Q61798011-34AAA4BE-E13D-4DBD-927D-E003E9D868AA wds:Q55334009-EF2E625C-A40C-4779-8EC0-93FC12F8D77C wds:Q35136414-6FD2CBD4-C818-4509-8220-528E1EB21CEA wds:Q35600804-0764866E-41C9-4FCD-A680-9AD782A83D40 wds:Q40092270-4B34A6D0-F28F-4685-9F99-98F06270E0DB

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