112023-27-5Relevant articles and documents
Diversity-oriented synthesis of fused thioglycosyl benzo[e][1,4]oxathiepin-5-ones and benzo[f][1,4]thiazepin-5(2H)-ones by a sequence of palladium-catalyzed glycosyl thiol arylation and deprotection-lactonization reactions
Al-Shuaeeb, Riyadh Ahmed Atto,Galvani, Gilles,Bernadat, Guillaume,Brion, Jean-Daniel,Alami, Mouad,Messaoudi, Samir
, p. 10904 - 10916 (2015)
An efficient synthesis of thioglycosylated benzo[e][1,4]oxathiepin-5-one and benzothiazepinone derivatives by a sequence of palladium-catalyzed glycosyl thiol arylation followed by deprotection-lactonization reactions has been reported. This diversity-oriented strategy enabled access to unknown complex cyclic scaffolds with polyhydroxylated appendages of biological interest.