About: DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones

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About: DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones Goto Sponge NotDistinct Permalink

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article by Yuhua Zhang & Chao-Jun Li published April 2006 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2006 (fr) наукова стаття, опублікована у квітні 2006 (uk) im April 2006 veröffentlichter wissenschaftlicher Artikel (de) 2006 ഏപ്രില്‍ 1 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം (ml) article by Yuhua Zhang & Chao-Jun Li published April 2006 in Journal of the American Chemical Society (en)
publication date	wds:Q55884226-2E242E31-67E8-445E-A46A-77BD2D9DF0CC
publication date	2006-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55884226-9226282E-4B8A-4960-AF05-5016C3177151
language of work or name	English
author name string	wds:Q55884226-031F4EB9-C9A5-4B5C-94F1-EE5F61421BE8 wds:Q55884226-1DE89C42-DC81-4E60-94BD-053895310082
author name string	Yuhua Zhang Chao-Jun Li
rdfs:label	DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones (en) DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (nl)
skos:prefLabel	DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones (en) DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (nl)
name	DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones (en) DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (nl)
title	wds:Q55884226-CE0C4A70-CE2A-4C01-BBB2-AAD8486E86B6
title	DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones (en)
page(s)	wds:Q55884226-8D4254FD-A77D-47A4-91E1-07268F6D7755
page(s)	4242-4243
instance of	wds:Q55884226-84FAF791-1224-49CE-9784-70CFA314F325
instance of	scholarly article
PubMed ID	wds:Q55884226-F69C6484-1EC9-4080-95CA-D0C59CAE988E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16568995
PubMed ID	16568995
published in	wds:Q55884226-657C1288-4A42-4412-9D83-40D86E90505F
published in	Journal of the American Chemical Society
issue	wds:Q55884226-398275DF-C04D-4BBD-BD98-8B64527F0685
volume	wds:Q55884226-CB600C3A-1C7F-4F85-8655-63A32152D0E7
issue	13
volume	128
DOI	wds:Q55884226-683FB771-0BA7-400E-BAA3-F6437AAE04C2
DOI	http://dx.doi.org/10.1021/JA060050P
DOI	10.1021/JA060050P
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55884226
is cites work of	Redox catalysis in organic electrosynthesis: basic principles and recent developments. The cross-dehydrogenative coupling of C(sp3)-H bonds: a versatile strategy for C-C bond formations Oxidative photoredox catalysis: mild and selective deprotection of PMB ethers mediated by visible light. Oxidative carbocation formation in macrocycles: synthesis of the neopeltolide macrocycle Bimolecular Coupling Reactions through Oxidatively Generated Aromatic Cations: Scope and Stereocontrol Enantioselective oxidative cross-dehydrogenative coupling of tertiary amines to aldehydes. Cyclization reactions through DDQ-mediated vinyl oxazolidinone oxidation Trifluoromethanesulfonic acid catalyzed synergetic oxidative/[3+2] cyclization of quinones with olefins Enantioselective copper-catalyzed alkynylation of benzopyranyl oxocarbenium ions Copper-catalyzed enantioselective additions to oxocarbenium ions: alkynylation of isochroman acetals Catalytic enantioselective oxidative cross-coupling of benzylic ethers with aldehydes. Remodeling of fumagillol: discovery of an oxygen-directed oxidative Mannich reaction Direct Sp3α-C-H activation and functionalization of alcohol and ether FeCl2-promoted cleavage of the unactivated C-C bond of alkylarenes and polystyrene: direct synthesis of arylamines. Efficient domino approaches to multifunctionalized fused pyrroles and dibenzo[b,e][1,4]diazepin-1-ones Iron-Facilitated Oxidative Dehydrogenative CO Bond Formation by Propargylic C sp 3H Functionalization An efficient palladium-catalyzed C-H alkoxylation of unactivated methylene and methyl groups with cyclic hypervalent iodine (i(3+) ) oxidants Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes. Efficient imidation of C(sp3)-H bonds adjacent to oxygen atoms of aryl ethers under metal-free conditions. Tandem C-H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (-)-brussonol and (-)-przewalskine E. The chemistry of organoimido derivatives of polyoxometalates Quinone-Catalyzed Selective Oxidation of Organic Molecules Nucleophilic attack of α-aminoalkyl radicals on carbon-nitrogen triple bonds to construct α-amino nitriles: an experimental and computational study. Di-tert-butyl peroxide-mediated atom-transfer radical addition of 2-chlorodithiane to aryl alkynes under mild conditions. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone-catalyzed reactions employing MnO2 as a stoichiometric oxidant Metal-Free Oxidative C-C Bond Formation through C-H Bond Functionalization. DDQ-catalyzed oxidative C--O coupling of sp³ C--H bonds with carboxylic acids Intramolecular hydride transfer onto arynes: redox-neutral and transition metal-free C(sp3)-H functionalization of amines. Organocatalytic Redox Deracemization of Cyclic Benzylic Ethers Enabled by An Acetal Pool Strategy. Copper catalyzed C-O bond formation via oxidative cross-coupling reaction of aldehydes and ethers. Transition-metal-free one-pot synthesis of biaryls from Grignard reagents and substituted cyclohexanones Aromatic cations from oxidative carbon-hydrogen bond cleavage in bimolecular carbon-carbon bond forming reactions Copper(I)-promoted cycloalkylation-peroxidation of unactivated alkenes via sp(3) C-H functionalisation. Synthesis of 2-oxindoles via 'transition-metal-free' intramolecular dehydrogenative coupling (IDC) of sp(2) C-H and sp(3) C-H bonds A multi-component domino reaction for the direct access to polyfunctionalized indoles via intermolecular allylic esterification and indolation Intermolecular cascade annulations of N-(arylsulfonyl)acrylamides with dual C(sp3)-H bonds: divergent access to indanes and pyrrolidin-2-ones. An iron-catalyzed hydroalkylation reaction of α,β-unsaturated ketones with ethers. A cascade coupling strategy for one-pot total synthesis of β-carboline and isoquinoline-containing natural products and derivatives Activation of CH Bonds through Oxidant-Free Photoredox Catalysis: Cross-Coupling Hydrogen-Evolution Transformation of Isochromans and β-Keto Esters Metal-free synthesis of allylic amines by cross-dehydrogenative-coupling of 1,3-diarylpropenes with anilines and amides under mild conditions Oxygenation of Simple Olefins through Selective Allylic C-C Bond Cleavage: A Direct Approach to Cinnamyl Aldehydes. Catalytic amounts of CBr4 mediated dehydrogenative coupling of isochromans with aromatic ketones. Oxidation-Initiated Cyclizations of Pentadienyl Ethers: An Alternative Entry to the Nazarov Reaction. Complementary Iron(II)-Catalyzed Oxidative Transformations of Allenes with Different Oxidants. Organocatalytic oxidative dehydrogenation of dihydroarenes by dioxygen using 2,3-dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2. Facile synthesis of benzo[b]thiophenes via metal-free radical-triggered intramolecular C-S bond formation. A Metal-Free Oxidative Dehydrogenative Diels-Alder Reaction for Selective Functionalization of Alkylbenzenes. The Ferraquinone-Ferrahydroquinone Couple: Combining Quinonic and Metal-Based Reactivity Toward Rational Understandings of α-C-H Functionalization: Energetic Studies of Representative Tertiary Amines DDQ-promoted direct transformation of benzyl hydrocarbons to amides via tandem reaction of the CDC reaction and Beckmann rearrangement. Gold-catalyzed reactions of 3-alkynyloxireno[2, 3-b]chromenones to form 3(2H)-furanones via a domino pathway Asymmetric Total Syntheses of Di- and Sesquiterpenoids by Catalytic C-C Activation of Cyclopentanones
is cites work of	wds:Q36770154-677C47D7-C9AE-4662-9ADB-07264FAF2BFA wds:Q51799696-864E936D-6AC6-407D-8098-25AC39F4E344 wds:Q45015241-CAC736BF-2614-416D-83B5-136B430034CD wds:Q55054476-874D4C8F-A31C-48B9-A52B-E47541A9C7B6 wds:Q37590541-AAB4C0D3-A3C3-4B7E-8015-1B29302EDD2A wds:Q54443958-6483DA91-D909-44E6-AC2D-C9EEE8EEC726 wds:Q36205893-C74AD974-FA32-47CF-A026-D748B7CF9FE6 wds:Q37058579-95EE967B-36C7-4EFC-AEF8-19EDE89AFBE2

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