ChemistrySelect · 2020 · 35 citations · 51 references
Abstract An environmentally benign, robust and straightforward protocol has been developed for the synthesis of a diverse array of 2,3‐dihydroquinazolin‐4(1 H )‐ones using 2‐aminobenzamide and various aldehydes or ketones. Water, a green solvent was adopted in this methodology replacing hazardous reaction mediums. Further, ascorbic acid, an organocatalyst has been accepted to meet the role of catalyst, thus bypassing the use of noxious metals or hazardous materials, which is another asset of this protocol. The activity of this novel methodology has been further being broadened using an oxidant oxone to synthesize 2‐substituted quinazolin‐4(3 H )‐one from aldehyde.
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De novo synthesis of substituted pyridines
Gavin D. Henry · Tetrahedron · 2004 · 700 citations
Mann‐Jen Hour, Li‐Jiau Huang, Sheng‐Chu Kuo et al. · Journal of Medicinal Chemistry · 2000 · 404 citations · Full text
Pharmaceutical Science, Chemoprevention Strategy, Organic Chemistry +18