1189369-68-3

Upstream product

• 1189369-54-7 (Z)-ethyl 2-(3-(3-(benzylamino)propyl)-5-methyl-4-oxothiazolidin-2-ylidene)acetate 
• 1189369-32-1 (Z)-ethyl 2-(3-(3-bromopropyl)-5-methyl-4-oxothiazolidin-2-ylidene)acetate 
• 105-56-6 ethyl 2-cyanoacetate 
• 26313-01-9 2-(4-oxo-5-methyl-2-thiazolidinylidene)acetic acid ethyl ester 

Relevant academic research and scientific papers

Endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines

endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations.