90559-99-2Relevant academic research and scientific papers
Hindered phenolic aminothiazoles – Synthesis, α-glucosidase and α-amylase inhibitory and antioxidant activities
Satheesh, Sandhya Vyjayanthy,Radha, Akhila Vijayan,Girija, Krishnapriya Krishnan Nair,Rajasekharan, Kallikat Narayanan,Maheswari, Priya Rani
, p. 1087 - 1095 (2017/11/16)
Base-catalysed heterocyclization of either N-aryl-N'-[imino(nitroamino)methyl]thioureas or N-aryl-N'-cyanothioureas by reaction with 2-bromo-1-(2,6-di-t-butyl-4-hydroxyphenyl)ethanone afforded 4-amino-2-(arylamino)--5-(3,5-di-t-butyl-4-hydroxybenzoyl)thia
One-pot sequential multicomponent route to 2,4-diaminothiazoles - A facile approach to bioactive agents for cancer therapeutics
Sreejalekshmi, Kumaran G.,Rajasekharan, Kallikat N.
supporting information; experimental part, p. 3627 - 3629 (2012/09/22)
A facile one-pot sequential three-component route to 2,4-diaminothiazoles is reported. The new approach employs the mildest reaction conditions and commercially available reagents to generate diverse 2-alkyl/arylamino-4-amino-5- aroyl/heteroylthiazoles in short reaction times, good yield, and purity.
Synthesis and antimicrobial studies of novel bis(diamino)thiazoles
Manju, Sreedharan L.,Devi, Satyabhama K. C.,Rajasekharan, Kallikat N.
scheme or table, p. 455 - 458 (2009/09/28)
(Chemical Equation Presented) The synthesis of novel bis(diamino)thiazoles has been achieved by reacting bis(bromoacetyl)benzene and 1-alkyl(or aryl)-3-(N-nitroamidino)thioureas in presence of triethylamine. These new compounds were characterized by spect
