Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.

Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.

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http://www.wikidata.org/entity/Q50495693
Waste as catalyst: tandem Wittig/conjugate reduction sequence to α-CF3 γ-keto esters that uses Ph3PO as catalyst for the chemoselective conjugate reduction.Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines.Catalyst-free synthesis of α1-oxindole-α-hydroxyphosphonates via phospha-aldol reaction of isatins employing N-heterocyclic phosphine (NHP)-thiourea.An efficient catalyst-free Mukaiyama-aldol reaction of fluorinated enol silyl ethers with tryptanthrin.Highly efficient "on water" catalyst-free nucleophilic addition reactions using difluoroenoxysilanes: dramatic fluorine effects.A catalyst-free, one-pot three-component aminomethylation of α-substituted nitroacetates: theoretical and experimental studies into the rate-accelerating effects of the solvent methanol.A highly efficient Friedel-Crafts reaction of tertiary α-hydroxyesters or α-hydroxyketones to α-quaternary esters or ketones.Copper-Catalyzed Reaction of Trifluoromethylketones with Aldehydes via a Copper Difluoroenolate.Palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines with isocyanides through double sp(2) C-H bonds cleavage: facile synthesis of 4-aminoquinoline derivatives.Efficient one-step synthesis of pyrrolo[3,4-c]quinoline-1,3-dione derivatives by organocatalytic cascade reactions of isatins and β-ketoamides.Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketiminesHighly stereoselective construction of adjacent tetrasubstituted carbon stereogenic centres via an organocatalytic Mukaiyama-aldol reaction of monofluorinated silyl enol ethers to isatinsAn Organocatalytic Addition of Nitromethane to Activated KetiminesA highly efficient thiourea catalyzed dehydrative nucleophilic substitution reaction of 3-substituted oxindoles with xanthydrolsCatalytic Asymmetric Construction of Stereogenic Carbon Centers that Feature agem-Difluoroalkyl GroupThe First Catalytic Asymmetric Morita-Baylis-Hillman Reaction of Acrolein with Aromatic AldehydesRecent advances in the application of deep eutectic solvents as sustainable media as well as catalysts in organic reactions
P2860

Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.

Item
http://www.wikidata.org/entity/Q50495693
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@en
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@nl
type
label
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@en
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@nl
prefLabel
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@en
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
Ethylene glycol: a powerful catalyst-free medium for C-C bond-forming reactions.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698