102736-27-6

Upstream product

• 108-98-5 thiophenol 
• 75-36-5 acetyl chloride 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 23326-27-4 Methyl 2-butynoate 
• 18913-35-4 methyl buta-2,3-dienoate 
• 616-42-2 dimethylsulfite 
• 67959-52-8 (2E)-3-(phenylthio)but-2-enoic acid 

Downstream Products

• 102736-42-5 dimethyl (Z)-3-(phenylthio)-5-(methoxycarbonyl)-2-adepate 
• 102736-43-6 dimethyl (E)-3-(phenylthio)-5-(methoxycarbonyl)-2-adepate 
• 102736-32-3 methyl 5-hydroxy-5-phenyl-3-(phenylthio)-pent-2-enoate 
• 102736-33-4 methyl 5-hydroxy-5-phenyl-3-(phenylthio)-pent-2-enoate 
• 102736-41-4 dimethyl 3-hydroxy-5-(phenylthio)-o-phthalate 
• 102736-31-2 methyl 4-(1-hydroxy-1-cyclohexyl)-3-(phenylthio)but-2-enoate 
• 102736-37-8 methyl 2-(phenylthio)-5,6,7,8-tetrahydronaphthalene-1-carboxylate 
• 102736-36-7 methyl 3-(phenylthio)-5,6,7,8-tetrahydronaphthalene-2-carboxylate 
• 102736-39-0 3-(phenylthio)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid 
• 102736-29-8 methyl 5-hydroxy-5-methyl-3-(phenylthio)hex-2-enoate 
• 102736-25-4 1-(trimethylsiloxy)-1-methoxy-3-(phenylthio)-1,3-butadiene 

Relevant academic research and scientific papers

Three-component reactions of phosphorus ylides, thiophenols, and acetyl chloride for the synthesis of (β-thioacrylates)

The facile synthesis of 2-thioacrylates has been realized via direct three-component reactions of thiophenols, Wittig reagents, and acetyl chloride. Under transition metal-free conditions, a class of 2-thioacrylates have been synthesized with fair to exce

Synthesis and evaluation of substrate analogues as mechanism-based inhibitors of type II isopentenyl diphosphate isomerase

(Chemical Equation Presented) Type 2 isopentenyl diphosphate isomerase (IDI-2), which catalyzes the interconversion of isopentenyl diphosphate and dimethylallyl diphosphate, contains a tightly bound molecule of FMN. To probe the mechanism of the reaction,

Chemoselective deoxygenation of sulfoxides with titanium tetraiodide

Chemoselective deoxygenation of sulfoxides was carried out using TiI4 as a reducing agent to give sulfides in good to excellent yields.

Experimental and Theoretical Study of the Radical-Chain Addition of Benzenethiol to Heterosubstituted Allenes

The radical-chain addition of benzenethiol to phenylallene (PHA), methoxyallene (MEOA), carbomethoxyallene (CBA), cyanoallene (CNA), chloroallene (ClA), and (phenylthio)- and allene (PHSA and MPHSA) has been studied.In all cases, exc

1-(Trimethylsiloxy)-1-methoxy-3--1,3-butadienes and the Synthesis of Aryl Sulfides via a Cycloaromatization Reaction

The preparation of 1-(trimethylsiloxy)-1-methoxy-3--1,3-butadienes and their Lewis acid catalyzed reactions with a number of carbonyl electrophiles are described.