26313-11-1

Upstream product

• 614-16-4 Benzoylacetonitrile 
• 623-51-8 ethyl 2-sulfanylacetate 

Downstream Products

• 615552-88-0 N-(5-phenyl-3H-1,2-dithiol-3-ylidene)ethanthioamide 
• 1258848-70-2 (Z)-2-bromo-2-(4-oxothiazolidin-2-ylidene)-1-phenylethanone 
• 1246177-59-2 (E)-2-bromo-2-(4-oxothiazolidin-2-ylidene)-1-phenylethanone 
• 26313-10-0 2-(2-oxo-2-phenyl-ethylidene)-thiazolidin-4-one 
• 1443772-33-5 (Z)-(3-methyl-1,4-dioxothiazolidin-2-ylidene)-1-phenylethanone 
• 1258848-63-3 (Z)-(3-benzyl-4-oxothiazolidin-2-ylidene)-1-phenylethanone 
• 1443772-38-0 (Z)-(3-benzyl-1,4-dioxothiazolidin-2-ylidene)-1-phenylethanone 
• 1410910-34-7 (Z)-3-(3-bromopropyl)-2-(2-oxo-2-phenylethylidene)-thiazolidin-4-one 

Relevant academic research and scientific papers

High-yield synthesis of substituted and unsubstituted pyridinium salts containing a 4-oxothiazolidine moiety

A new series of unsubstituted and substituted pyridinium salts bearing a 4-oxothiazolidinyl moiety has been prepared by an efficient rearrangement of 2-(l-bromoalkylidene)thiazolidin-4-ones. The process is based on three steps, namely carbon - bromine cle

Mechanism of stereoselective synthesis of push-pull (Z)-4-oxothiazolidine derivatives containing an exocyclic double bond. A MNDO-PM3 Study

Calculations using the MNDO-PM3 method were performed to elucidate the mechanism of stereoselective base-catalyzed reaction affording exclusively (Z)-2-alkylidene-4-oxothiazolidine push-pull derivatives from the corresponding α-mercapto esters and activated β-oxonitriles in ethanol as a solvent.