1609182-71-9Relevant academic research and scientific papers
Easy access to α-hydroxyimino-β-oxodithioesters and application towards the synthesis of diverse 1,4-thiazine-3-ones via reduction/annulation cascade
Nagaraju, Anugula,Shukla, Gaurav,Srivastava, Abhijeet,Ramulu, B. Janaki,Verma, Girijesh Kumar,Raghuvanshi, Keshav,Singh, Maya Shankar
, p. 3740 - 3746 (2014/05/20)
An operationally simple and facile synthesis of α-hydroxyimino- β-oxodithioesters has been achieved by nitrosation of α- enolicdithioesters. They were further treated with internal alkynes to afford diverse 1,4-thiazin-3-ones via domino reduction/annulati
A facile and straightforward synthesis of 1,2,3-thiadiazoles from α-enolicdithioesters via nitrosation/reduction/diazotization/cyclization cascade in one-pot
Nagaraju, Anugula,Ramulu, B. Janaki,Shukla, Gaurav,Srivastava, Abhijeet,Verma, Girijesh Kumar,Raghuvanshi, Keshav,Singh, Maya Shankar
, p. 2430 - 2433 (2014/05/06)
An operationally simple, economical, and straightforward synthesis of diverse 4,5-disubstituted 1,2,3-thiadiazoles from α-enolicdithioesters has been achieved via nitrosation/reduction/diazotization/cyclization sequence in one-pot through the formation of cascade 1-2 (N-S) and 3-4 (C-N) bonds. Importantly, this is the first straightforward entry to highly functionalized 1,2,3-thiadiazoles from dithioesters.
