Saha, Debasmita published the artcileA sequential synthetic strategy towards unexplored dibenzo[b,f][1,4]thiazepine carboxamides: copper catalyzed C-S cyclization followed by Ugi type 3CC cascade, Category: chlorides-buliding-blocks, the main research area is carboxamide dibenzothiazepine preparation; dibenzothiazepine preparation isocyanide carboxylic acid Ugi reaction; aminothiophenol halo benzaldehyde copper catalyst cyclization.
A two-step diversity oriented synthetic protocol to a novel class of dihydrodibenzo[b,f][1,4]thiazepine-11-carboxamides was developed. The first step ensured the synthesis of dibenzothiazepine via copper-mediated condition followed by Ugi-Joullie reaction of the resultant cyclic imine in the second step.
RSC Advances published new progress about Amides Role: SPN (Synthetic Preparation), PREP (Preparation). 93118-03-7 belongs to class chlorides-buliding-blocks, name is 2-Chloro-3-(trifluoromethyl)benzaldehyde, and the molecular formula is C8H4ClF3O, Category: chlorides-buliding-blocks.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics