845779-13-7Relevant academic research and scientific papers
The ammonia-free partial reduction of substituted pyridinium salts
Donohoe, Timothy J.,Johnson, Dale J.,MacE, Laura H.,Thomas, Rhian E.,Chiu, Jessica Y. K.,Rodrigues, Jason S.,Compton, Richard G.,Banks, Craig E.,Tomcik, Peter,Bamford, Mark J.,Ichihara, Osamu
, p. 1071 - 1084 (2007/10/03)
This paper reports a study into the partial reduction of N-alkylpyridinium salts together with subsequent elaboration of the intermediates thus produced. Activation of a pyridinium salt by placing an ester group at C-2, allows the addition of two electron
Partial reduction of pyridinium salts as a versatile route to dihydropyridones
Donohoe, Timothy J.,Johnson, Dale J.,Mace, Laura H.,Bamford, Mark J.,Ichihara, Osamu
, p. 435 - 437 (2007/10/03)
(Chemical Equation Presented) The addition of two electrons to a pyridinium salt turns it into a nucleophile. The intermediate generated by the reduction of such salts can be reacted successfully with a range of different electrophiles (acids, alkyl halid
