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References from Metal-Free C–H Functionalization of Allenamides: An Access to Branched Allylic Esters. Local targets link to admitted publications; unresolved targets remain external evidence.
Aromatic constituents of Uvaria grandiflora
10.1021/np050500b · 2006 · External reference
The Discodermolide Hairpin Structure Flows from Conformationally Stable Modular Motifs
10.1021/jm9015284 · 2010 · External reference
Antitubercular and Cytotoxic Chlorinated seco-Cyclohexenes from Uvaria alba
10.1021/acs.jnatprod.7b00679 · 2017 · External reference
Palladium-Catalyzed Isocyanide Insertion with Allylic Esters: Synthesis of N-(But-2-enoyl)-N-(tert-butyl)benzamide Derivatives via Intramolecular Acyl Transfer Termination
10.1002/adsc.201700765 · 2017 · External reference
Hydroamination versus Allylic Amination in Iridium-Catalyzed Reactions of Allylic Acetates with Amines: 1,3-Aminoalcohols via Ester-Directed Regioselectivity
10.1021/jacs.8b05683 · 2018 · External reference
N-Heterocyclic Carbene/Palladium Cascade Catalysis: Construction of 2,2-Disubstitiuted Benzofuranones from the Reaction of 3-(2-Formylphenoxy) propenoates with Allylic Esters
10.1021/acs.joc.7b02849 · 2018 · External reference
Iron-catalyzed boration of allylic esters: an efficient approach to allylic boronates
10.1039/c7qo00228a · 2017 · External reference
Catalytic Asymmetric Synthesis of Chiral Allylic Esters
10.1021/ja106685w · 2010 · External reference
Copper catalyzed asymmetric synthesis of chiral allylic esters
10.1021/ja065780b · 2006 · External reference
Enantioselective Synthesis of Allylic Esters via Asymmetric Allylic Substitution with Metal Carboxylates Using Planar-Chiral Cyclopentadienyl Ruthenium Catalysts
10.1021/ja908456b · 2010 · External reference
CBr4 promoted intramolecular aerobic oxidative dehydrogenative arylation of aldehydes: application in the synthesis of xanthones and fluorenones
10.1039/c7ob00080d · 2017 · External reference
Fluorous biphasic esterification directed towards ultimate atom efficiency
10.1002/1521-3773(20021104)41:21<4117::aid-anie4117>3.0.co;2-4 · 2002 · External reference
Serial ligand catalysis: A highly selective allylic C-H oxidation
10.1021/ja0500198 · 2005 · External reference
A sulfoxide-promoted, catalytic method for the regioselective synthesis of allylic acetates from monosubstituted olefins via C-H oxidation
10.1021/ja039107n · 2004 · External reference
Synthetic Versatility in C-H Oxidation: A Rapid Approach to Differentiated Diols and Pyrans from Simple Olefins
10.1021/ja206013j · 2011 · External reference
Branch-Selective Allylic C-H Carboxylation of Terminal Alkenes by Pd/sox Catalyst
10.1021/ol5019135 · 2014 · External reference
Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic C-H Esterification
10.1021/ol201314m · 2011 · External reference
Macrolactonization via hydrocarbon oxidation
10.1021/ja063096r · 2006 · External reference
Allylic Oxidation of Alkenes Catalyzed by a Copper-Aluminum Mixed Oxide
10.1021/ol500198c · 2014 · External reference
Cu(CH3CN)(4)PF6 immobilized on halloysite as efficient heterogeneous catalyst for oxidation of allylic C-H bonds in olefins under mild reaction condition
10.1007/s11164-019-03745-z · 2019 · External reference
Novel N,N-Bidentate Ligands for Enantioselective Copper(I)-Catalyzed Allylic Oxidation of Cyclic Olefins
10.1002/adsc.200800457 · 2008 · External reference
Copper-catalyzed oxidative coupling of acids with alkanes involving dehydrogenation: facile access to allylic esters and alkyl alkenes
10.1039/c4cc09393c · 2015 · External reference
Copper porphyrin as efficient catalysts for esterification of allyl sp(3) C-H bond with carboxylic acid
10.1016/j.catcom.2019.04.001 · 2019 · External reference
Copper-catalyzed enantioselective allylic oxidation of acyclic olefins
10.1016/j.tetlet.2013.03.046 · 2013 · External reference
Copper-catalyzed oxidative esterification of unactivated C(sp(3))-H bonds with carboxylic acids via cross dehydrogenative coupling
10.1039/c4ra14586k · 2015 · External reference
Copper-catalyzed regioselective allylic oxidation of olefins via C-H activation
10.1016/j.tetlet.2017.09.047 · 2017 · External reference
Iron-catalyzed esterification of allylic sp(3) C-H bonds with carboxylic acids: Facile access to allylic esters
10.1016/j.tetlet.2017.05.039 · 2017 · External reference
Enantioselective Redox-Neutral Rh-Catalyzed Coupling of Terminal Alkynes with Carboxylic Acids Toward Branched Allylic Esters
10.1021/jacs.5b01131 · 2015 · External reference
Atom economic macrolactonization and lactonization via redox-neutral rhodium-catalyzed coupling of terminal alkynes with carboxylic acids
10.1039/c2sc00812b · 2012 · External reference
Redox-Neutral Atom-Economic Rhodium-Catalyzed Coupling of Terminal Alkynes with Carboxylic Acids Toward Branched Allylic Esters
10.1021/ja1108613 · 2011 · External reference
Palladium-catalyzed hydrocarboxylation of allenes
10.1021/ja974223+ · 1998 · External reference
Iridium-catalyzed hydrocarboxylation of 1,1-dimethylallene: Byproduct-free reverse prenylation of carboxylic acids
10.1021/ol702914p · 2008 · External reference
Enantioselective Synthesis of Branched Allylic Esters via Rhodium-Catalyzed Coupling of Allenes with Carboxylic Acids
10.1021/ja210149g · 2011 · External reference
Tetrabutylammonium Iodide Catalyzed Synthesis of Allylic Ester with tert-Butyl Hydroperoxide as an Oxidant
10.1021/ol3013606 · 2012 · External reference
Synthesis of amido-spiro 2.2 pentanes via Simmons-Smith cyclopropanation of allenamides
10.1039/b908205k · 2009 · External reference
Allenamides: A Powerful and Versatile Building Block in Organic Synthesis
10.1021/cr400015d · 2013 · External reference
Cycloaddition chemistry of allenamides
2010 · External reference
The emergence of allenamides in organic synthesis
10.1021/ar030029i · 2003 · External reference
An intermolecular iodoamination of allenamides with sulfonamides mediated by N-iodosuccinimide
10.1016/j.tetlet.2016.09.020 · 2016 · External reference
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides
10.1039/c6cc05046h · 2016 · External reference
Regioselective 1,2-addition of allenamides with N-haloimides: synthesis of 2-halo allylic aminal derivatives
10.1039/c7ob00882a · 2017 · External reference
NIS-Mediated intermolecular hydroamination of allenamides with imidazole heterocycles: a facile protocol for the synthesis of allylic N,N-acetals
10.1039/c8nj03641a · 2018 · External reference
Regioselective 1,2-additions of alcohols to allenamides mediated by N-Iodosuccinimide: Synthesis of N,O-aminals
10.1016/j.tet.2018.07.045 · 2018 · External reference
Intermolecular [2+2] reaction of N-allenylsulfonamides with vinylarenes: enantioselective gold(I)-catalyzed synthesis of cyclobutane derivatives
10.1002/anie.201206461 · 2012 · External reference
Intermolecular Hydroalkoxylation of N-Allenyl Sulfonamides with Oximes Catalyzed by Cationic Gold(I) Salts
10.1055/s-0035-1560399 · 2016 · External reference
[3+2]-Annulation of platinum-bound azomethine ylides with distal C=C bonds of N-allenamides
10.1039/c6cc07874e · 2017 · External reference
Organocatalyzed Intermolecular Asymmetric Allylic Dearomatization of Both alpha- and beta-Naphthols
10.1021/acs.orglett.8b03934 · 2019 · External reference
Taming gold(I)-counterion interplay in the de-aromatization of indoles with allenamides
10.1002/chem.201403155 · 2014 · External reference
Formal Intermolecular [2+2] Cycloaddition Reaction of Alleneamides with Alkenes via Gold Catalysis
10.1021/ol202703a · 2012 · External reference
Enantioselective Synthesis of trans-Vicinal Diamines viaRhodium-Catalyzed [2+2] Cycloaddition of Allenamides
10.1002/adsc.201800021 · 2018 · External reference
Rhodium-Catalyzed Regio- and Stereoselective [2+2] Cycloaddition of Allenamides
10.1021/acs.orglett.6b01731 · 2016 · External reference
Cesium hydroxide-catalyzed isomerization of terminal alkynes for the synthesis of O-allenes and N-allenes
10.1016/j.tetlet.2015.08.016 · 2015 · External reference
Efficient preparations of novel ynamides and allenamides
10.1016/s0040-4020(00)01014-0 · 2001 · External reference