alkenes has been researched along with 2-oxindole in 46 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (6.52) | 29.6817 |
2010's | 43 (93.48) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barbas, CF; Bui, T; Syed, S | 1 |
Chen, Z; Furutachi, M; Kato, Y; Matsunaga, S; Mitsunuma, H; Shibasaki, M | 1 |
Castaldi, MP; Porco, JA; Troast, DM | 1 |
Selvakumar, K; Shanmugam, P; Vaithiyanathan, V | 1 |
Nagasawa, H; Okada, T; Ueda, S | 1 |
Ding, M; Qian, ZQ; Zhou, F; Zhou, J | 1 |
Duan, XH; Dufour, J; Jaegli, S; Neuville, L; Piou, T; Vors, JP; Wei, HL; Zhu, J | 1 |
Dufour, J; Neuville, L; Piou, T; Wei, HL; Zhu, J | 1 |
Chen, WB; Du, XL; Han, YY; Wu, ZJ; Yuan, WC; Zhang, XM | 1 |
Chang, Y; Chen, G; Di, Y; Gao, S; Hao, X; He, H; Li, S; Lu, Y; Yang, J | 1 |
Du, XL; Liao, YH; Liu, XL; Wu, ZJ; Yuan, WC; Zhang, XM | 1 |
Geng, ZC; Huang, XF; Liu, ZM; Wang, XW; Wang, Y; Zhang, SY | 1 |
Jin, CY; Liu, YZ; Shen, C; Wang, Y; Xu, PF | 1 |
Dou, X; Han, X; Lu, Y; Meng, Y; Yao, W; Zhong, F; Zhu, Q | 1 |
Fan, JH; Hu, M; Li, JH; Liu, W; Liu, Y; Song, RJ; Wei, WT; Xie, P; Zhou, MB | 1 |
Antonchick, AP; Matcha, K; Narayan, R | 1 |
Hu, P; Li, X; Xiao, X; Xu, X; Zhou, C | 1 |
Krische, MJ; Luong, T; Mowat, J; Yamaguchi, E | 1 |
Duan, XH; Guo, LN; Meng, Y; Wang, H | 1 |
Banerjee, D; Besnard, C; Jia, YX; Katayev, D; Kündig, EP; Sharma, AK; Sunoj, RB | 1 |
Cui, BD; Han, WY; Wu, ZJ; Yuan, WC; Zhang, XM | 1 |
Dou, X; Lu, Y; Yao, W; Zhou, B | 1 |
Li, JH; Liu, Y; Song, RJ; Wang, CY; Wei, WT; Zhou, MB | 1 |
Li, XA; Li, YM; Wei, XH; Yang, SD | 1 |
Jiao, N; Shen, T; Yuan, Y | 1 |
Battistini, L; Casiraghi, G; Curti, C; Pelosi, G; Ranieri, B; Rassu, G; Sartori, A; Zanardi, F | 1 |
Feng, H; Hou, W; Li, Y; Yang, Y; Zhou, B | 1 |
Chen, Q; Jiang, X; Lin, L; Wang, G; Wang, R; Xu, Z | 1 |
Jiao, N; Shen, T; Song, S; Yuan, Y | 1 |
Bao, Y; Su, YM; Wang, JY; Wang, XS; Xu, YM; Yin, F; Zhang, X | 1 |
Dong, R; Guo, M; Liu, X; Wang, H; Wei, W; Wen, J; Yang, D | 1 |
Bao, X; Ma, Y; Qu, J; Song, Y; Wang, B; Zou, L | 1 |
Fu, H; Shi, L; Wang, Y; Yang, H | 1 |
Loh, TP; Lu, MZ | 1 |
He, Z; Li, R; Liu, Y; Yang, C; Zhou, R | 1 |
Guo, CC; Jiang, Q; Sheng, WB; Tian, M; Yin, Y; Zhang, MZ | 1 |
A Attanasi, O; A Campisi, L; De Crescentini, L; Favi, G; Mantellini, F | 1 |
Cui, BD; Wu, ZJ; Xu, XY; You, Y; Yuan, WC; Zhang, XM; Zhao, JQ; Zuo, J | 1 |
Fang, H; Gao, Y; Li, X; Tang, G; Xu, J; Zhao, Y | 1 |
Chen, L; Xu, XY; You, Y; Yuan, WC; Zhang, ML; Zhang, XM; Zhao, JQ; Zuo, J | 1 |
Cheng, JP; Li, X; Li, Z; Wang, F; Wang, J | 1 |
Gao, F; Xia, W; Xu, Z; Yang, C; Zheng, L | 1 |
Ahamad, S; Gupta, AK; Gupta, E; Kant, R; Mohanan, K | 1 |
Chen, S; Krische, MJ; Luong, T; McInturff, EL; Qu, K | 1 |
Chen, JY; Chen, T; Gou, XT; He, SH; Jiang, Y; Long, RY; Luo, N; Shi, WB; Zhang, MZ | 1 |
Agalave, SG; Bisht, GS; Chaudhari, MB; Gnanaprakasam, B; Kanyal, A; Karmodiya, K; Pandey, AM | 1 |
46 other study(ies) available for alkenes and 2-oxindole
Article | Year |
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Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine.
Topics: Alkenes; Catalysis; Cholinesterase Inhibitors; Indoles; Molecular Structure; Nitro Compounds; Oxindoles; Physostigmine; Stereoisomerism; Thiourea | 2009 |
A homodinuclear Mn(III)2-Schiff base complex for catalytic asymmetric 1,4-additions of oxindoles to nitroalkenes.
Topics: Alkenes; Catalysis; Cyclization; Indoles; Molecular Structure; Nitro Compounds; Oxindoles; Schiff Bases; Stereoisomerism | 2009 |
Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations.
Topics: Alkenes; Cyclization; Indoles; Isatin; Oxepins; Oxindoles; Propanols; Pyrans; Silanes; Spiro Compounds; Stereoisomerism | 2009 |
An efficient stereoselective synthesis of 3-spirocyclopentene- and 3-spiropyrazole-2-oxindoles via 1,3-dipolar cycloaddition reaction.
Topics: Alkenes; Cyclization; Indoles; Models, Molecular; Molecular Structure; Oxindoles; Pyrazoles; Spiro Compounds; Stereoisomerism | 2010 |
Oxindole synthesis by palladium-catalysed aromatic C-H alkenylation.
Topics: Alkenes; Catalysis; Cyclization; Indoles; Oxindoles; Palladium | 2010 |
Organocatalytic Michael addition of unprotected 3-substituted oxindoles to nitroolefins.
Topics: Alkenes; Catalysis; Indoles; Nitrogen; Oxindoles; Stereoisomerism; Substrate Specificity | 2010 |
Palladium-catalyzed carbo-heterofunctionalization of alkenes for the synthesis of oxindoles and spirooxindoles.
Topics: Alkenes; Catalysis; Cyclization; Indoles; Oxidation-Reduction; Oxindoles; Palladium; Spiro Compounds | 2010 |
Iodo-carbocyclization of electron-deficient alkenes: synthesis of oxindoles and spirooxindoles.
Topics: Alkenes; Cyclization; Electrons; Indoles; Molecular Structure; Oxindoles; Spiro Compounds | 2011 |
Diastereo- and enantioselective conjugate addition of 3-substituted oxindoles to nitroolefins catalyzed by a chiral Ni(OAc)2-diamine complex under mild conditions.
Topics: Alkenes; Catalysis; Indoles; Ligands; Molecular Structure; Nickel; Nitro Compounds; Organometallic Compounds; Oxindoles; Stereoisomerism | 2011 |
Spiro[pyrrolidine-2,3'-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions.
Topics: Alkenes; Amino Acids; Chemistry, Organic; Crystallography, X-Ray; Cyclization; Indoles; Isatin; Magnetic Resonance Spectroscopy; Oxindoles; Pyrrolidines; Spiro Compounds; Stereoisomerism | 2012 |
Organocatalytic asymmetric conjugate addition of 3-monosubstituted oxindoles to (E)-1,4-diaryl-2-buten-1,4-diones: a strategy for the indirect enantioselective furanylation and pyrrolylation of 3-alkyloxindoles.
Topics: Alkenes; Catalysis; Cinchona Alkaloids; Cyclization; Indoles; Molecular Structure; Oxindoles; Stereoisomerism | 2012 |
Enantioselective construction of multifunctionalized spirocyclohexaneoxindoles through organocatalytic Michael-Aldol cyclization of isatin derived alkenes with linear dialdehydes.
Topics: Aldehydes; Alkenes; Catalysis; Cyclization; Cyclohexanes; Indoles; Isatin; Models, Molecular; Oxindoles; Spiro Compounds; Stereoisomerism | 2012 |
Organocatalytic asymmetric Michael addition of oxindoles to nitroolefins for the synthesis of 2,2-disubstituted oxindoles bearing adjacent quaternary and tertiary stereocenters.
Topics: Alkenes; Catalysis; Chemistry Techniques, Synthetic; Indoles; Nitro Compounds; Oxindoles; Stereoisomerism | 2012 |
Chiral phosphine catalyzed asymmetric Michael addition of oxindoles.
Topics: Alkenes; Amino Acids; Catalysis; Indoles; Oxindoles; Phosphines; Stereoisomerism | 2013 |
Synthesis of oxindoles by iron-catalyzed oxidative 1,2-alkylarylation of activated alkenes with an aryl C(sp2)-H bond and a C(sp3)-H bond adjacent to a heteroatom.
Topics: Alkenes; Carbon; Catalysis; Ethers; Hydrogen; Indoles; Iron; Kinetics; Oxidation-Reduction; Oxindoles; Quantum Theory | 2013 |
Metal-free radical azidoarylation of alkenes: rapid access to oxindoles by cascade C-N and C-C bond-forming reactions.
Topics: Alkenes; Azides; Carbon; Free Radicals; Indoles; Metals; Nitrogen; Oxindoles; Temperature | 2013 |
Synthesis of sulfonated oxindoles by potassium iodide catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides in water.
Topics: Alkenes; Catalysis; Hydrazines; Indoles; Molecular Structure; Oxindoles; Potassium Iodide; Sulfonic Acids; Water | 2013 |
Regio- and diastereoselective C-C coupling of α-olefins and styrenes to 3-hydroxy-2-oxindoles by Ru-catalyzed hydrohydroxyalkylation.
Topics: Alkenes; Catalysis; Hydrogenation; Indoles; Oxindoles; Ruthenium; Stereoisomerism | 2013 |
Metal-free oxidative hydroxyalkylarylation of activated alkenes by direct sp3 C-H functionalization of alcohols.
Topics: Alcohols; Alkenes; Cyclization; Indoles; Molecular Structure; Oxidation-Reduction; Oxindoles | 2013 |
Synthesis of 3,3-Disubstituted Oxindoles by Palladium-Catalyzed Asymmetric Intramolecular α-Arylation of Amides: Reaction Development and Mechanistic Studies.
Topics: Alkenes; Amides; Catalysis; Indoles; Ligands; Methane; Molecular Structure; Oxindoles; Palladium; Stereoisomerism | 2013 |
Enantioselective synthesis of quaternary 3-aminooxindoles via organocatalytic asymmetric Michael addition of 3-monosubstituted 3-aminooxindoles to nitroolefins.
Topics: Alkenes; Amines; Catalysis; Indoles; Molecular Structure; Nitro Compounds; Oxindoles; Stereoisomerism | 2013 |
Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene.
Topics: Alkenes; Amines; Aza Compounds; Catalysis; Indoles; Oxindoles; Stereoisomerism; Thiourea | 2013 |
Oxidative 1,2-difunctionalization of activated alkenes with benzylic C(sp3)-H bonds and aryl C(sp2)-H bonds.
Topics: Alkenes; Cyclohexanes; Indoles; Molecular Structure; Oxidation-Reduction; Oxindoles | 2013 |
Metal-free carbonitration of alkenes using K2S2O8.
Topics: Alkenes; Catalysis; Indoles; Nitro Compounds; Oxidation-Reduction; Oxindoles; Potassium Compounds; Sulfates | 2013 |
Metal-free nitro-carbocyclization of activated alkenes: a direct approach to synthesize oxindoles by cascade C-N and C-C bond formation.
Topics: Alkenes; Carbon; Cyclization; Indoles; Metals; Nitrogen; Oxidation-Reduction; Oxindoles | 2014 |
3-Alkenyl-2-silyloxyindoles in vinylogous Mannich reactions: synthesis of aminated indole-based scaffolds and products.
Topics: Alkenes; Catalysis; Indoles; Lewis Acids; Molecular Structure; Oxindoles; Silanes; Stereoisomerism | 2014 |
Copper(I)-catalyzed aryl or vinyl addition to electron-deficient alkenes cascaded by cationic cyclization.
Topics: Alkenes; Catalysis; Cations; Copper; Cyclization; Electrons; Indoles; Molecular Structure; Oxindoles; Physostigmine; Stereoisomerism | 2014 |
Highly enantioselective organocatalyzed vinylogous Michael-type reaction for the construction of trifluoromethylated all-carbon quaternary stereocenters.
Topics: Alkenes; Carbon; Catalysis; Hydrocarbons, Fluorinated; Indoles; Molecular Structure; Nitro Compounds; Oxindoles; Stereoisomerism | 2014 |
Iron-catalyzed aerobic difunctionalization of alkenes: a highly efficient approach to construct oxindoles by C-S and C-C bond formation.
Topics: Air; Alkenes; Catalysis; Indoles; Iron; Oxidants; Oxindoles; Oxygen; Sulfinic Acids; Sulfones | 2014 |
Pd(0)-Catalyzed radical aryldifluoromethylation of activated alkenes.
Topics: Acrylamides; Alkenes; Catalysis; Hydrocarbons, Fluorinated; Indoles; Methylation; Oxindoles; Palladium; Sulfones | 2014 |
Metal-free direct trifluoromethylation of activated alkenes with Langlois' reagent leading to CF3-containing oxindoles.
Topics: Alkenes; Chlorofluorocarbons, Methane; Indoles; Methylation; Molecular Conformation; Oxindoles | 2014 |
Novel tartrate-derived guanidine-catalyzed highly enantio- and diastereoselective Michael addition of 3-substituted oxindoles to nitroolefins.
Topics: Alkenes; Catalysis; Guanidine; Indoles; Nitro Compounds; Oxindoles; Stereoisomerism; Substrate Specificity; Tartrates | 2014 |
Copper-catalyzed bis-arylations of alkenes leading to oxindole derivatives.
Topics: Alkenes; Catalysis; Copper; Indoles; Oxindoles | 2014 |
Iron-catalyzed cascade carbochloromethylation of activated alkenes: highly efficient access to chloro-containing oxindoles.
Topics: Alkenes; Carbon Tetrachloride; Catalysis; Ferrous Compounds; Hydrocarbons, Chlorinated; Indoles; Methylene Chloride; Molecular Structure; Oxidants; Oxindoles | 2014 |
Diastereoselective synthesis of functionalized spirocyclopropyl oxindoles via P(NMe2)3-mediated reductive cyclopropanation.
Topics: Alkenes; Cyclopropanes; Electrons; Indoles; Isatin; Molecular Structure; Oxindoles; Stereoisomerism | 2014 |
Metal-free synthesis of oxindoles via (NH4)2S2O8-mediated halocarbocyclization of alkenes in water.
Topics: Alkenes; Catalysis; Hydrocarbons, Halogenated; Indoles; Metals; Oxindoles; Water | 2014 |
Synthesis of novel symmetrical 2-oxo-spiro[indole-3,4'-pyridines] by a reaction of oxindoles with 1,2-diaza-1,3-dienes.
Topics: Alkenes; Chemistry Techniques, Synthetic; Indoles; Oxindoles; Pyridines; Spiro Compounds | 2015 |
3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives.
Topics: Alkenes; Catalysis; Indoles; Nitro Compounds; Oxindoles; Pyrroles | 2015 |
Cascade arylalkylation of activated alkenes: synthesis of chloro- and cyano-containing oxindoles.
Topics: Acetates; Acetonitriles; Alkenes; Catalysis; Cyclization; Indoles; Molecular Structure; Organometallic Compounds; Oxidation-Reduction; Oxindoles; Spiro Compounds | 2015 |
Organocatalytic asymmetric Michael addition of 3-substituted oxindoles to α,β-unsaturated acyl phosphonates for the synthesis of 3,3'-disubstituted oxindoles with chiral squaramides.
Topics: Alkenes; Amides; Catalysis; Indoles; Organophosphonates; Oxindoles; Stereoisomerism | 2015 |
Enantioselective Synthesis of Dihydropyran-Fused Indoles through [4+2] Cycloaddition between Allenoates and 3-Olefinic Oxindoles.
Topics: Alkenes; Catalysis; Cycloaddition Reaction; Indoles; Lewis Bases; Oxindoles; Pyrans; Spiro Compounds; Stereoisomerism | 2015 |
Difunctionalization of Alkenes via the Visible-Light-Induced Trifluoromethylarylation/1,4-Aryl Shift/Desulfonylation Cascade Reactions.
Topics: Alkenes; Catalysis; Hydrocarbons, Fluorinated; Indoles; Isoquinolines; Light; Molecular Structure; Oxindoles; Sulfhydryl Compounds | 2015 |
Substrate-controlled product-selectivity in the reaction of the Bestmann-Ohira reagent with N-unprotected isatin-derived olefins.
Topics: Alkenes; Cyclization; Indoles; Isatin; Molecular Structure; Organophosphonates; Oxindoles; Pyrazoles; Stereoisomerism | 2015 |
Ruthenium(0)-Catalyzed C-C Coupling of Alkynes and 3-Hydroxy-2-oxindoles: Direct C-H Vinylation of Alcohols.
Topics: Alcohols; Alkenes; Alkynes; Catalysis; Coordination Complexes; Hydrogenation; Ligands; Molecular Structure; Oxidation-Reduction; Oxindoles; Ruthenium; Stereoisomerism; Temperature | 2017 |
Transition-Metal-Free Oxidative Aminooxyarylation of Alkenes: Annulations toward Aminooxylated Oxindoles.
Topics: Alkenes; Indoles; Molecular Structure; Oxidation-Reduction; Oxindoles | 2018 |
Ru-Catalyzed dehydrogenative synthesis of antimalarial arylidene oxindoles.
Topics: Alkenes; Antimalarials; Catalysis; Chemistry Techniques, Synthetic; Hydrogenation; Inhibitory Concentration 50; Oxindoles; Plasmodium falciparum; Ruthenium | 2018 |