A novel I 2 -catalyzed one-pot multicomponent protocol for the synthesis of a variety of elusive furo[2,3-b] pyrrole and thieno[2,3-b]pyrrole libraries has been established. To date, cyclization among alkanone, hydrazine and 2-bromobenzofuran or 2-bromobenzo[b]thiophene has not been explored in one-pot. Thus, the proposed single step protocol provides a versatile alternative to existing routes for accessing useful furo[2,3-b]pyrrole and thieno[2,3-b]pyrrole libraries.

A novel synthesis of N-fused imino-1,2,4-thiadiazolo derivatives is described. This approach involves the inexpensive, nontoxic, recoverable, and easy to handle montmorillonite K10 that catalyzes the coupling of 3-aminoisoquinolines and phenylisothiocyanates to afford the N-fused imino-1,2,4-thiadiazolo isoquinoline motifs in exemplary yields. The main attractions of this synthetic strategy were simple procedure and excellent yields.

A novel library of aminomethylphenol has been developed using magnetic Fe 3 O 4 nanoparticles via Petasis borono-Mannich reaction of salicylaldehydes, secondary amines and phenyl boronic acids. This one-pot protocol features mild reaction conditions, excellent yields in short reaction times, readily available starting materials, good functional group tolerance and reusability of the catalyst for four consecutive cycles without significant loss in its activity.

No abstract

No abstract