About: Mild Rhodium(III)-Catalyzed C-H Activation and Intermolecular Annulation with Allenes

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scholarly article by Honggen Wang & Frank Glorius published 18 April 2012 in Angewandte Chemie International Edition

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована у квітні 2012 (uk) im April 2012 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Honggen Wang & Frank Glorius published 18 April 2012 in Angewandte Chemie International Edition (en)
publication date	wds:Q57657269-50354E88-F0C8-4EC1-85D3-B92E40D41C34
publication date	2012-04-18 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57657269-8EA51E48-69C5-45F7-BBCD-64A8C5520E56
language of work or name	English
cites work	wds:Q57657269-0627EB87-D3CD-455A-B9F5-505077E1A8A6 wds:Q57657269-084F5A1F-B083-4901-AC93-605168E3D0B0 wds:Q57657269-0BE59734-A6FC-44FC-BFB0-7EA83B081250 wds:Q57657269-1B22A020-59AA-44D1-9F8F-5BBC03C80F3B wds:Q57657269-1D4F868A-C6DE-4E99-9AAC-4CE229D9D861 wds:Q57657269-20674E0D-9CBD-46AE-B028-A98D4C6AA972 wds:Q57657269-24BC2820-7E8E-45C2-9DE4-EF644EACA844 wds:Q57657269-340F36DE-7D29-4588-93B4-444300C9398E wds:Q57657269-3A6CAF33-BD68-408C-90BA-F91CDD71FF3C wds:Q57657269-45E1D107-5838-4316-85FB-372F0E513029 wds:Q57657269-46CB7140-DAA0-4501-9B7D-6E605A2F2268 wds:Q57657269-4E205378-A708-40FE-BB1C-7C8BF0BBBFAF wds:Q57657269-58FC8C09-4A54-424C-A84C-FA33C6CFCEDD wds:Q57657269-5A809BF1-14F0-4DB3-9129-D2C538C80853 wds:Q57657269-63431A1C-A12E-40C1-8649-92FE4FB48FCB wds:Q57657269-6A24AEB7-8CC8-4BF4-8C28-E682EA390083 wds:Q57657269-6DBEDA21-D082-4951-A5C6-B5A8DCA6312F wds:Q57657269-6F882169-9D3D-4A75-A0B5-5270AA8C190B wds:Q57657269-7632E8F2-9395-40B9-A4E2-9816D23427B5 wds:Q57657269-7B3295EE-C61D-4D07-B38E-C2E78FD44D3A wds:Q57657269-7EBAB2DE-8968-4E70-BC19-B95F426DC14F wds:Q57657269-8A43D946-B092-4D16-A64C-3B9740B91750 wds:Q57657269-8AC478D1-3EA3-4B9E-A3A2-7E32BACD60B4 wds:Q57657269-96519C8A-D2EA-42F6-95D9-416B8DD7016C wds:Q57657269-97FDB761-BDDB-42DE-8ADA-8B6D07F03591 wds:Q57657269-9A556249-642D-438C-B601-40540E6302BC wds:Q57657269-A06EAD85-C90E-4A44-807E-61282F2AA73F wds:Q57657269-A07378B1-B8C5-459A-9195-8852718B070B wds:Q57657269-A4648721-36B5-463B-8204-23D6BAD1B6BD wds:Q57657269-C05CFF48-3D9E-4C49-9A9A-B296A9514A84 wds:Q57657269-C153F842-CA76-4FCF-A743-90CA5B94A452 wds:Q57657269-D08E0921-8871-4312-94C1-2CE286CCAF92 wds:Q57657269-D2AA7613-1BB3-43E0-B337-3813A6923D31 wds:Q57657269-E026D005-34FD-4707-97BB-12BADECA1B5F wds:Q57657269-E298F374-2136-4B8B-B64D-CFF43987142C wds:Q57657269-E4B907E5-A806-4655-867F-C63C7F251953 wds:Q57657269-F19B94E8-11F0-43D9-8D25-F48AB4E73455 wds:Q57657269-F93D8DF3-3C4B-4C2A-A965-EE1E2A3B91C2 wds:Q57657269-FE6683F5-3E3E-4164-AC61-98ED52759BBC
cites work	Structure-activity relationship analysis of novel derivatives of narciclasine (an Amaryllidaceae isocarbostyril derivative) as potential anticancer agents Rhodium(III)-catalyzed arylation of Boc-imines via C-H bond functionalization Rhodium-catalyzed direct addition of aryl C-H bonds to N-sulfonyl aldimines. Towards mild metal-catalyzed C-H bond activation Rh catalyzed olefination and vinylation of unactivated acetanilides Oxidative coupling of aromatic substrates with alkynes and alkenes under rhodium catalysis. Palladium-catalyzed alkenylation of quinoline-N-oxides via C-H activation under external-oxidant-free conditions Pd(II)-catalyzed cross-coupling of sp3 C-H Bonds with sp2 and sp3 boronic acids using air as the oxidant Rh(III)-catalyzed oxidative coupling of unactivated alkenes via C-H activation Mechanism of the rhodium(III)-catalyzed arylation of imines via C-H bond functionalization: inhibition by substrate Pyridinyl directed alkenylation with olefins via Rh(III)-catalyzed C-C bond cleavage of secondary arylmethanols. Rhodium-catalyzed oxidative ortho-acylation of benzamides with aldehydes: direct functionalization of the sp2 C-H bond. Rhodium-catalyzed oxidative cycloaddition of benzamides and alkynes via C-H/N-H activation An efficient waste-free oxidative coupling via regioselective C-H bond cleavage: Rh/Cu-catalyzed reaction of benzoic acids with alkynes and acrylates under air. Pyridine synthesis from oximes and alkynes via rhodium(III) catalysis: Cp* and Cp(t) provide complementary selectivity Rhodium(III)-catalyzed synthesis of isoquinolines from aryl ketone O-acyloxime derivatives and internal alkynes. Rh(III)-Catalyzed Directed C−H Olefination Using an Oxidizing Directing Group: Mild, Efficient, and Versatile Computational Elucidation of the Internal Oxidant-Controlled Reaction Pathways in Rh(III)-Catalyzed Aromatic C–H Functionalization Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation Rhodium(III)-catalyzed oxidative carbonylation of benzamides with carbon monoxide Rhodium-katalysierte oxidative Olefinierung von C-H-Bindungen in Acetophenonen und Benzamiden Rhodium(III)-catalyzed isoquinolone synthesis: the N-O bond as a handle for C-N bond formation and catalyst turnover Synthesis of heterocycles via palladium-catalyzed oxidative addition. Expedient synthesis of N-acyl anthranilamides and β-enamine amides by the Rh(III)-catalyzed amidation of aryl and vinyl C-H bonds with isocyanates Transition Metal-Catalyzed [5 + 2] Cycloadditions of Allenes and Vinylcyclopropanes: First Studies of Endo−Exo Selectivity, Chemoselectivity, Relative Stereochemistry, and Chirality Transfer Pyrrole synthesis via allylic sp3 C-H activation of enamines followed by intermolecular coupling with unactivated alkynes Palladium-catalyzed amination of aromatic C-H bonds with oxime esters Fluorescent naphthyl- and anthrylazoles from the catalytic coupling of phenylazoles with internal alkynes through the cleavage of multiple C-H bonds. Diverse Strategies toward Indenol and Fulvene Derivatives: Rh-Catalyzed C−H Activation of Aryl Ketones Followed by Coupling with Internal Alkynes The Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles Rh[III]-Catalyzed Direct C–H Amination Using N-Chloroamines at Room Temperature Oxidierende dirigierende Gruppen ermöglichen effiziente und innovative C-H-Aktivierungsreaktionen Rh(III)-catalyzed tandem oxidative olefination-Michael reactions between aryl carboxamides and alkenes. [RhIIICp*]-Catalyzed Dehydrogenative ArylAryl Bond Formation Synthesis of some members of the hydroxylated phenanthridone subclass of the Amaryllidaceae alkaloid family Rhodium-catalyzed mono- and divinylation of 1-phenylpyrazoles and related compounds via regioselective C-H bond cleavage RhIII-Catalyzed Oxidative Olefination of Vinylic CH Bonds: Efficient and Selective Access to Di-unsaturated α-Amino Acid Derivatives and Other Linear 1,3-Butadienes Rh Catalyzed C–H Activation and Oxidative Olefination without Chelate Assistance: On the Reactivity of Bromoarenes A Facile method to transform trans-4-carboxy-3,4-dihydro-3-phenyl- 1(2H)-isoquinolones to indeno[1,2-c]isoquinolines
author name string	wds:Q57657269-61B0C91B-F71E-446C-99B2-1CBA4AEFCCF2
author name string	Honggen Wang
rdfs:label	Mild Rhodium(III)-Catalyzed C-H Activation and Intermolecular Annulation with Allenes (en)
skos:prefLabel	Mild Rhodium(III)-Catalyzed C-H Activation and Intermolecular Annulation with Allenes (en)
name	Mild Rhodium(III)-Catalyzed C-H Activation and Intermolecular Annulation with Allenes (en)
author	wds:Q57657269-A39C99F0-B84B-47F9-AA53-4DB3F9FC6188
author	Frank Glorius
title	wds:Q57657269-03B7FA88-E584-4BC1-BA92-0DF10D57C8F4
title	Mild Rhodium(III)-Catalyzed C-H Activation and Intermolecular Annulation with Allenes (en)
page(s)	wds:Q57657269-905C5CB1-92BF-4F6F-9529-BF39886D7C11
page(s)	7318-7322
instance of	wds:Q57657269-AE025C0D-4767-4680-9708-728DFF7D7F53

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