86357-87-1

Upstream product

• 37510-42-2 3,3-bis(ethylthio)-1-phenylprop-2-en-1-one 
• 98-80-6 phenylboronic acid 
• 7338-94-5 1,3-diphenyl-2-propynone 
• 75-08-1 ethanethiol 

Downstream Products

• 52762-76-2 (Z,E)-1,3,5-triphenyl-penta-2,4-dien-1-one 
• 99143-01-8 1t.3-diphenyl-1c-p-tolyl-propen-⁽¹⁾-one-⁽³⁾ 
• 99142-94-6 1c.3-diphenyl-1t-p-tolyl-propen-⁽¹⁾-one-⁽³⁾ 
• 39092-22-3 4-(4-chlorophenyl)-4-phenylbut-3-en-2-one 

Relevant academic research and scientific papers

BF3·Et2O promoted conjugate addition of ethanethiol to electron-deficient alkynes

An effective method for the synthesis of vinyl thioethers through the conjugate addition of ethanethiol to electron-deficient alkynes promoted by BF3·Et2O has been developed. Electron-deficient internal alkynes react with ethanethiol

Tributylphosphine-catalyzed reaction of ethanethiol with alkynyl ketones

A stereoselective and effective method for the synthesis of vinyl thioethers has been developed. This method is based on the Michael addition of ethanethiol to various alkynyl ketones using 10 mol% of tributylphosphine as catalyst. Most of alkynyl ketones

Regio- and stereoselective synthesis of multisubstituted olefins and conjugate dienes by using α-oxo ketene dithioacetals as the building blocks

An efficient palladium(0)-catalyzed, Cu(I)-mediated synthetic route to trisubstituted olefins and conjugate dienes has been developed via oxo directing Liebeskind-Srogl cross-coupling reactions of gem-dihaloolefin-type α-oxo ketene dithioacetals with aryl