About: Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry

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About: Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry Goto Sponge NotDistinct Permalink

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scientific article published on 31 May 2019

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) artículu científicu espublizáu en mayu de 2019 (ast) im Mai 2019 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 31 May 2019 (en) наукова стаття, опублікована 31 травня 2019 (uk)
publication date	wds:Q92946145-1047BDEA-2E1F-4C32-AD4D-EAEDC4C1ECD5
publication date	2019-05-31 00:00:00Z (xsd:dateTime)
cites work	wds:Q92946145-07470DA5-4535-445E-B6BA-3126FED8A1DA wds:Q92946145-0BF5A13C-4D9C-4FBB-9250-4117E59CA93D wds:Q92946145-20CD9EA0-C0CC-4C3C-B05A-8EE958C57AB8 wds:Q92946145-2F92FB50-477E-417E-B80E-30A04A6789B0 wds:Q92946145-3071485C-6370-44B5-B49C-8519748643DF wds:Q92946145-34269086-84BD-43D7-B66E-783931699014 wds:Q92946145-37F4917D-89BA-4C42-AB64-98FE09BB623D wds:Q92946145-46509000-191A-4033-A27B-BF57045C152C wds:Q92946145-49CECB0F-2AE8-4737-B5E0-D374A2A211C9 wds:Q92946145-5302CA0F-988A-404A-BF06-6BACAA495BEF wds:Q92946145-55268919-119D-4756-B226-CCDC60F2572A wds:Q92946145-55B823E8-0EA9-4063-8228-DFAEC270CD4E wds:Q92946145-57972D9B-4978-4EFA-A804-0D2D0A95AC89 wds:Q92946145-58B7E7B1-FD27-494F-89FD-DAF8EB72EF35 wds:Q92946145-6373AB4A-BBCD-4959-8CFD-96E5A5483FBB wds:Q92946145-75B95C0B-7025-4DF6-B6AF-E21869C030E7 wds:Q92946145-81493EE8-F605-4097-B2F4-A8C66964A072 wds:Q92946145-82316820-2882-49C8-B448-D78C296BC392 wds:Q92946145-868FB4DD-4C6C-42D1-BCEE-F27560A9F5C4 wds:Q92946145-8922856E-976E-465A-93AC-89D29CDD04FC wds:Q92946145-8C9B13B8-E2E3-4988-AD1F-DC80369868BA wds:Q92946145-940F8983-51F5-40AE-87FD-385DD99ADFDB wds:Q92946145-95FC0C98-4AFC-432B-9B75-DD5A40965D61 wds:Q92946145-ADDA4B87-57DE-45AC-8BFF-A6B121C4E7CD wds:Q92946145-B19A976D-56F0-4CE7-B4D8-7A27459628B1 wds:Q92946145-C6259F35-0C3F-481C-95C6-B0B72F53C057 wds:Q92946145-CD75284E-D514-4BF3-B32A-FFD748E79A03 wds:Q92946145-DA013B26-7987-4AD4-95D0-8B57A197DEB0 wds:Q92946145-EF50C7FE-A99F-46D1-B0DE-9DAD4C59FA17 wds:Q92946145-F15B5F08-58C9-435E-A5FC-BC7690FD0ABA wds:Q92946145-F51CD32C-A187-45B3-A119-3D4CAC5FEECC wds:Q92946145-F9158BD6-9F4F-43C5-B9D3-3343B8A9442A
cites work	Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks Recent advances in organocatalytic asymmetric Morita-Baylis-Hillman/aza-Morita-Baylis-Hillman reactions Multifunctional chiral phosphine organocatalysts in catalytic asymmetric Morita-Baylis-Hillman and related reactions. Organocatalytic asymmetric transformations of modified Morita-Baylis-Hillman adducts Transition metal-catalyzed carbon-carbon bond activation Metal-catalysed cleavage of carbon-carbon bonds Metal Insertion into C-C Bonds in Solution Metal-free tandem oxidative aryl migration and C-C bond cleavage: synthesis of α-ketoamides and esters from acrylic derivatives The enantioselective Morita-Baylis-Hillman reaction and its aza counterpart The Baylis-Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry. Construction of chiral quaternary carbon through Morita-Baylis-Hillman reaction: an enantioselective approach to 3-substituted 3-hydroxyoxindole derivatives Organocatalytic asymmetric synthesis of substituted 3-hydroxy-2-oxindoles via Morita-Baylis-Hillman reaction. Catalytic, asymmetric Baylis-Hillman reaction of imines with methyl vinyl ketone and methyl acrylate Enantioselective Morita-Baylis-Hillman reaction of isatins with acrylates: facile creation of 3-hydroxy-2-oxindoles Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons Chemoselective oxidative C(CO)-C(methyl) bond cleavage of methyl ketones to aldehydes catalyzed by CuI with molecular oxygen Catalytic reactions involving the cleavage of carbon-cyano and carbon-carbon triple bonds Biochemical and pharmacological characterization of isatin and its derivatives: from structure to activity Morita-Baylis-Hillman adduct derivatives (MBHADs): versatile reactivity in Lewis base-promoted annulation A one-pot copper catalyzed biomimetic route to N-heterocyclic amides from methyl ketones via oxidative C-C bond cleavage Copper-catalyzed aerobic oxidative inert C-C and C-N bond cleavage: a new strategy for the synthesis of tertiary amides. Tertiary amine-catalyzed chemoselective and asymmetric [3 + 2] annulation of Morita-Baylis-Hillman carbonates of isatins with propargyl sulfones α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation Highly enantioselective [3 + 2]-annulation of isatin-derived morita-baylis-hillman adducts with cyclic sulfonimines Catalyst-Controlled Switch in Chemo- and Diastereoselectivities: Annulations of Morita-Baylis-Hillman Carbonates from Isatins Copper-catalyzed aerobic oxidative C-C bond cleavage of unstrained ketones with air and amines. Transition-metal-free aerobic oxidative cleavage of C-C bonds in α-hydroxy ketones and mechanistic insight to the reaction pathway. Copper-catalyzed aerobic oxidative C-C bond cleavage for C-N bond formation: from ketones to amides The Morita-Baylis-Hillman reaction: insights into asymmetry and reaction mechanisms by electrospray ionization mass spectrometry. Diastereo- and enantioselective [3 + 2] cycloaddition reaction of Morita-Baylis-Hillman carbonates of isatins with N-phenylmaleimide catalyzed by Me-DuPhos Enantioselective synthesis of 3,3'-dihydropyrryl-spirooxindoles via an organocatalytic three-component reaction From ketones to esters by a Cu-catalyzed highly selective C(CO)-C(alkyl) bond cleavage: aerobic oxidation and oxygenation with air
author name string	wds:Q92946145-082EC4C2-12A0-4253-83EA-74195D866813 wds:Q92946145-5FD97832-0859-40B9-8E19-8E0D7A1E34BC wds:Q92946145-87DC3230-0E05-4AE9-8BFE-AC5771CCDA2E wds:Q92946145-A10CD0EF-52AE-4F25-A309-1D5F74363B52 wds:Q92946145-F19F3620-ED5F-4DD3-A41F-F6520A0EF6FD
author name string	Ezhumalai Vellikannu Ravichandran Ganesan Thirumailavan Vijayakumar Vaithiyanathan Vadivel Vishnu Kannaiyan
rdfs:label	Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (en) Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (nl)
skos:prefLabel	Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (en) Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (nl)
name	Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (en) Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (nl)
title	wds:Q92946145-8E0947A1-8E70-428E-99EB-49D10CC25D6D
title	Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection-Deprotection Chemistry (en)
page(s)	wds:Q92946145-41CDBF2B-122E-4764-B45F-80A6AACEE640
page(s)	9563-9568
instance of	wds:Q92946145-387D4383-5852-42C8-9B5C-8DA4E22B9823
instance of	scholarly article
PubMed ID	wds:Q92946145-B75D88ED-3B50-40DE-9A5C-A4F61887B670
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31460047
PubMed ID	31460047
published in	wds:Q92946145-907F3861-CBF8-4DAC-8F39-81FE1F4975AE
published in	ACS Omega
issue	wds:Q92946145-D1F842EB-17E4-49E4-A694-7DB475D716C8

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