Claisen type Condensation of Methyl Ketones with Carbimidothioates: A New Gateway for the Synthesis of β‐Enaminones

2021 ◽  
Vol 6 (2) ◽  
pp. 177-180
Author(s):  
Toreshettahally R. Swaroop ◽  
Kanchugarakoppal S. Rangappa ◽  
Lokman Torun
Keyword(s):  
Author(s):  
Joseph N. Capilato ◽  
Peter J Pellegrinelli ◽  
Josephine Bernard ◽  
Logan Schnorbus ◽  
Shane Philippi ◽  
...  

The development of a novel acetyl nitrate mediated oxidative conversion of methyl ketones to carboxylic acid derivatives is described. By analogy to the haloform reaction and supported by experimental and...


Synlett ◽  
2020 ◽  
Vol 31 (14) ◽  
pp. 1430-1434
Author(s):  
Ming Bian ◽  
Jin-feng Zhou ◽  
Dong-min Tang

An efficient and practical protocol for the geminal heterodihalogenation of methyl ketones by using readily available dimethyl sulfoxide and a combination of HCl and HBr is reported. Control experiments suggested that the acidity of the solution, as well as the oxidizing ability and nucleophilicity of the dimethyl sulfoxide might work cooperatively in ensuring the success of the tandem substitution. Its operational simplicity, easy accessibility, and mild oxidative conditions suggest that the present strategy might be useful for the assembly of bromochloromethyl functional groups in drug discovery.


2013 ◽  
Vol 125 (43) ◽  
pp. 11384-11384
Author(s):  
Lin Zhang ◽  
Xihe Bi ◽  
Xiaoxue Guan ◽  
Xingqi Li ◽  
Qun Liu ◽  
...  

1946 ◽  
Vol 68 (7) ◽  
pp. 1386-1388 ◽  
Author(s):  
Howard G. Walker ◽  
Charles R. Hauser
Keyword(s):  

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