83300-58-7

Upstream product

• 14572-78-2 lithium tris(phenylthio)methanide 
• 78-94-4 methyl vinyl ketone 
• 61971-73-1 2,2-dichlorocyclopropyl methyl ketone 
• 108-98-5 thiophenol 
• 930-69-8 sodium thiophenolate 

Downstream Products

• 147915-77-3 (E)-1-(2,2-Bis-phenylsulfanyl-cyclopropyl)-3-(4-nitro-phenyl)-propenone 
• 147915-78-4 4-[(E)-3-(2,2-Bis-phenylsulfanyl-cyclopropyl)-3-oxo-propenyl]-benzoic acid methyl ester 
• 86816-42-4 C₁₈H₁₈S₂ 
• 147915-88-6 1-((1E,3E)-6,6-Bis-phenylsulfanyl-hexa-1,3,5-trienyl)-4-bromo-benzene 
• 147915-76-2 (E)-1-(2,2-Bis-phenylsulfanyl-cyclopropyl)-3-(4-bromo-phenyl)-propenone 
• 147915-75-1 (E)-1-(2,2-Bis-phenylsulfanyl-cyclopropyl)-3-phenyl-propenone 
• 83300-70-3 5,5-Bis-phenylsulfanyl-pent-4-en-2-one 
• 86816-52-6 2-(2,2-Bis-phenylsulfanyl-cyclopropyl)-propan-2-ol 

Relevant academic research and scientific papers

SYNTHESIS OF DIPHENYLTHIOACETALS OF POLYCONJUGATED KETENES FROM GEM-DI(PHENYLTHIO)CYCLOPROPYL KETONES

The condensation of methyl gem-di(phenylthio)cyclopropyl ketones and substituted benzaldehydes gave a series of 1-(3-arylpropenoyl)-2,2-di(phenylthio)cyclopropanes.The reduction of these cyclopropanes with sodium borohydride and subsequent dehydration of

A Novel One-Flask Cyclopropanation and Vinylcyclopropanation Method for α-Enones. Copper(I)-Induced γ-Thiophenoxide Removal from Conjugate Adducts

A novel concept for performing a one-flak cyclopropanation of conjugated enones consists of conjugate addition of an appropriate phenylthio-stabilized organolithium compound followed by treatment of the resulting enolate anion with cuprous trifluoromethan

SYNTHESIS AND ISOMERIZATION OF 1-ACYL-2,2-DI(PHENYLTHIO)CYCLOPROPANES

The reaction of 1-acyl-2,2-dichlorocyclopropanes with sodium thiophenolate in methanol leads to the products from nucleophilic substitution of the chlorine atoms with retention of the cyclopropane ring.The obtained 1-acyl-2,2-di(phenylthio)cyclopropanes i