A highly efficient Friedel-Crafts reaction of 3-hydroxyoxindoles and aromatic compounds to 3,3-diaryl and 3-alkyl-3-aryloxindoles catalyzed by Hg(ClO4)2·3H2O.

A highly efficient Friedel-Crafts reaction of 3-hydroxyoxindoles and aromatic compounds to 3,3-diaryl and 3-alkyl-3-aryloxindoles catalyzed by Hg(ClO4)2·3H2O.

Item
http://www.wikidata.org/entity/Q50506949
Preparation of Aryl-Susbstituted 2-Oxyindoles by Superelectrophilic Chemistry.Organocatalytic asymmetric Michael addition of unprotected 3-substituted oxindoles to 1,4-naphthoquinoneSynergistic dual activation catalysis by palladium nanoparticles for epoxide ring opening with phenols.Synthesis of 3,3-disubstituted oxindoles by one-pot integrated Brønsted base-catalyzed trichloroacetimidation of 3-hydroxyoxindoles and Brønsted acid-catalyzed nucleophilic substitution reaction.α-Carbonyl Cations in Sulfoxide-Driven Oxidative Cyclizations.Synthesis of α-functionalized α-indol-3-yl carbonyls through direct SN reactions of indol-3-yl α-acyloins.Transition-metal-free Chemoselective Oxidative C-C Coupling of the sp3 C-H Bond of Oxindoles with Arenes and Addition to Alkene: Synthesis of 3-Aryl Oxindoles, and Benzofuro- and Indoloindoles.A highly enantioselective Hg(ii)-catalyzed Sakurai-Hosomi reaction of isatins with allyltrimethylsilanes.A highly efficient Friedel-Crafts reaction of tertiary α-hydroxyesters or α-hydroxyketones to α-quaternary esters or ketones.A catalytic metal-free Ritter reaction to 3-substituted 3-aminooxindoles.Me-BIPAM for the Synthesis of Optically Active 3-Aryl-3-hydroxy-2-oxindoles by Ruthenium-catalyzed Addition of Arylboronic Acids to IsatinsAn Organocatalytic Addition of Nitromethane to Activated KetiminesA highly efficient thiourea catalyzed dehydrative nucleophilic substitution reaction of 3-substituted oxindoles with xanthydrolsThe First Catalytic Asymmetric Morita-Baylis-Hillman Reaction of Acrolein with Aromatic Aldehydes
P2860

A highly efficient Friedel-Crafts reaction of 3-hydroxyoxindoles and aromatic compounds to 3,3-diaryl and 3-alkyl-3-aryloxindoles catalyzed by Hg(ClO4)2·3H2O.

Item
http://www.wikidata.org/entity/Q50506949
description
2011 nî lūn-bûn
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2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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2011年學術文章
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name
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@en
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@nl
type
label
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@en
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@nl
prefLabel
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@en
A highly efficient Friedel-Cra ...... s catalyzed by Hg(ClO4)2·3H2O.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
A highly efficient Friedel-Cra ...... es catalyzed by Hg(ClO4)2·3H2O
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698