41563-50-2

Upstream product

• 83078-46-0 2-Methyl-dithiopropionsaeure-phenylester 
• 981-18-0 triphenyl(phenylazo)methane 
• 15821-77-9 Aluminium tris(phenylthiolate) 
• 79-31-2 isobutyric Acid 
• 13307-76-1 [bis(phenylthio)methyl]lithium 
• 69190-58-5 (bis-phenylsulfanyl-methyl)-boronic acid 
• 14572-78-2 lithium tris(phenylthio)methanide 
• 108-98-5 thiophenol 
• 14758-40-8 1,1,1-tris(phenylthio)-2-methylpropane 

Downstream Products

• 13640-71-6 2-methyl-1-(phenylthio)-1-propene 
• 157954-49-9 1,1-Bis(phenylthio)-2-methyl-1-octen-4-ol 
• 157954-37-5 6,6-Bis(phenylthio)-5-methyl-5-hexen-3-ol 
• 157954-40-0 1,1-Bis(phenylthio)-2-methyl-1-hepten-4-ol 
• 71342-11-5 2-Methyl-3-phenylsulfanyl-dec-2-en-4-ol 
• 60582-26-5 3-methyl-2-phenylthio-2-butenoic acid 
• 71342-12-6 1-(2-Methyl-1-phenylsulfanyl-propenyl)-cyclohexanol 
• 157955-34-5 1,1-Bis(phenylthio)-2-methyl-1-nonen-4-yl acetate 
• 163069-05-4 6-(3-methyl-2-phenylthiobutenyl)-1,4-dioxaspiro<4,5>decane 
• 163068-80-2 2-methyl-2-(4-methyl-3-phenylthiopenten-3-yl)-1,3-dioxolane 
• 157955-28-7 4,4-Bis(phenylthio)-3-methyl-1-phenyl-3-butenyl acetate 
• 157955-31-2 1,1-Bis(phenylthio)-2-methyl-1-octen-4-yl acetate 

Relevant academic research and scientific papers

A General Preparative Method for Carbonyl-Protected γ-Lithioketones via Reductive Lithiation. Synthetic Uses of the Bishomoenolate Equivalents

The mixed cuprates, generated by reductive lithiation of bis(phenylthio)acetals using lithium 4,4'-di-tert-butylbiphenylide (LDBB), followed by addition of cuprous bromide-dimethyl sulfide complex, undergo conjugate addition to enones in the presence of t

ELIMINATION OF THIOPHENOL FROM PHENYL ORTHOTHIOESTERS IN THE MASS SPECTROMETER AND NOVEL REARRANGEMENT OF KETENE THIOACETALS UPON ELECTRON IMPACT

The mass spectra of four selected phenyl orthothioesters (1-4) have been measured.The obtained spectra revealed the conversion of the compounds (1-4) into ketene thioacetals (5-8) via the elimination of thiophenol in the mass spectrometer.The thermal natu