Zn Mediated Chemoselective Allylation of Keto Esters with Allylic Halides in Aqueous Medium

1996 ◽  
Vol 25 (1) ◽  
pp. 95-95
Keyword(s):  
Aqueous Medium ◽  
Keto Esters ◽  
Allylic Halides

Zn Mediated Chemoselective Allylation of Keto Esters with Allylic Halides in Aqueous Medium

1995 ◽  
Vol 24 (5) ◽  
pp. 341-342 ◽  
Author(s):  
Matthias Ahonen ◽  
Rainer Sjöholm
Keyword(s):  
Aqueous Medium ◽  
Keto Esters ◽  
Allylic Halides

scholarly journals Retraction of “Oxone-Mediated Oxidative Cleavage of β-Keto Esters and 1,3-Diketones to α-Keto Esters and 1,2-Diketones in Aqueous Medium”

2020 ◽  
Vol 85 (2) ◽  
pp. 1324-1324 ◽  
Author(s):  
Anastasios Stergiou ◽  
Anna Bariotaki ◽  
Dimitris Kalaitzakis ◽  
Ioulia Smonou
Keyword(s):  
Aqueous Medium ◽  
Oxidative Cleavage ◽  
Keto Esters

Oxone-Mediated Oxidative Cleavage of β-Keto Esters and 1,3-Diketones to α-Keto Esters and 1,2-Diketones in Aqueous Medium

2013 ◽  
Vol 78 (14) ◽  
pp. 7268-7273 ◽  
Author(s):  
Anastasios Stergiou ◽  
Anna Bariotaki ◽  
Dimitris Kalaitzakis ◽  
Ioulia Smonou
Keyword(s):  
Aqueous Medium ◽  
Oxidative Cleavage ◽  
Keto Esters

ChemInform Abstract: Oxone-Mediated Oxidative Cleavage of β-Keto Esters and 1,3-Diketones to α-Keto Esters and 1,2-Diketones in Aqueous Medium.

ChemInform ◽  
2013 ◽  
Vol 44 (49) ◽  
pp. no-no
Author(s):  
Anastasios Stergiou ◽  
Anna Bariotaki ◽  
Dimitris Kalaitzakis ◽  
Ioulia Smonou
Keyword(s):  
Aqueous Medium ◽  
Oxidative Cleavage ◽  
Keto Esters

One-Pot Telescoped Synthesis of Thiazole Derivatives from β-Keto Esters and Thioureas Promoted by Tribromoisocyanuric Acid

Synthesis ◽  
2018 ◽  
Vol 50 (24) ◽  
pp. 4867-4874 ◽  
Author(s):  
Marcio de Mattos ◽  
Vitor de Andrade
Keyword(s):  
Aqueous Medium ◽  
Thiazole Derivatives ◽  
One Pot ◽  
Keto Esters ◽  
Single Process

A simple and efficient one-pot protocol has been developed for the synthesis of thiazole derivatives from readily available starting materials. Tribromoisocyanuric acid was successfully used for α-monohalogenation of β-keto esters in aqueous medium, which in the presence of thiourea and DABCO produced the corresponding 2-aminothiazoles in up to 87% yield. Extension of the reaction to thioacetamide and o-phenylenediamine led to 2-methylthiazole and quinoxalines, respectively. This approach enables telescoping of the two steps into a single process.

Photoredox-Catalyzed Intramolecular Cyclopropanation of Alkenes with α-Bromo-β-keto Esters

2021 ◽  
Author(s):  
Kohta Ide ◽  
Miyu Furuta ◽  
Hidetoshi Tokuyama
Keyword(s):  
Aqueous Medium ◽  
Radical Addition ◽  
Reaction Process ◽  
Sequential Reaction ◽  
Keto Esters

Mild photoredox-catalyzed intramolecular cyclopropanation of alkenes with α-bromo-β-keto esters in an aqueous medium was developed. The sequential reaction process comprising intramolecular radical addition of α-bromo-β-keto esters to olefins under photoredox...

Rheological behaviour of the condensed suspension of fluorinated montmorillonite “rassoul” particles in aqueous medium

2005 ◽  
Vol 123 ◽  
pp. 341-344
Author(s):  
A. Khaldoun ◽  
F. González-Caballero ◽  
J. G. López-Durán ◽  
N. Mahrach ◽  
M. L. Kerkeb
Keyword(s):  
Aqueous Medium ◽  
Rheological Behaviour
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