The development of catalytic carbonylation reactions has increased considerably. Although
many reviews/chapters/books on carbonylation reactions have been published, summaries …

In heterocyclic chemistry, amidoximes are mostly known as precursors for the synthesis of 1,
2, 4-oxadiazoles. Indeed, most of the works related to the use of amidoximes in the synthesis …

Recent advances in the carbonylative synthesis of heterocycles by using diverse CO
surrogates as sources of CO are summarized and discussed. The merger of carbonylative …

An environmentally benign and convenient strategy for the synthesis of 4, 5-disubstituted/N-
fused 3-amino-1, 2, 4-triazoles and 3-substituted 5-amino-1, 2, 4-thiadiazoles from …

1, 2, 4-Oxadiazole is one of the important heterocycles used by medicinal chemists in
designing a new therapeutic molecule. The compounds containing this nucleus are reported …

Written by highly renowned and experienced authors, this is the only reference on the
application of solvents as reagents. Clearly structured, the text describes various methods …

A palladium-catalyzed three-component carbonylative reaction of
trifluoroacetimidohydrazides and aryl iodides for the synthesis of pharmaceutically valuable …

A novel and expeditious approach for the synthesis of N-fused and 3, 4-disubstituted 5-imino-
1, 2, 4-thiadiazole derivatives has been achieved through the molecular iodine-catalyzed …

A one‐pot synthesis of 1, 2, 4‐oxadiazoles has been achieved from the corresponding
amidoximes and carboxylic acids or from nitriles, hydroxylamine and carboxylic acids …

A facile and efficient approach to access 1, 2, 4‐triazolo [4, 3‐a] pyridines and related
heterocycles has been accomplished through condensation of readily available aryl …