52042-22-5

Upstream product

• 103-30-0 (E)-1,2-diphenyl-ethene 
• 140-89-6 potassium ethyl xanthogenate 
• 1439-07-2 (S,S)-trans-stilbene oxide 
• 645-49-8 cis-stilben 
• 588-59-0 stilbene 
• 52042-22-5 trans-4,5-diphenyl-1,5-dithiolan-2-thione 

Downstream Products

• 3795-75-3 (1R,2S)-1,2-Diphenyl-ethane-1,2-dithiol 
• 645-49-8 cis-stilben 
• 82204-49-7 Trithiocarbonic acid (E)-1,2-diphenyl-vinyl ester methyl ester 
• 103-30-0 (E)-1,2-diphenyl-ethene 

Relevant academic research and scientific papers

Convenient synthesis of 1,3-dithiolane-2-thiones: Cyclic trithiocarbonates as conformational locks

A series of novel 1,3-dithiolane-2-thiones, or cyclic trithiocarbonates, has been prepared by a new simple procedure: a treatment of the corresponding epoxides with the commercially available potassium ethyl xanthogenate, KSC(S)OEt. The stereochemistry of the products was determined by 1H NMR and in some cases by single-crystal X-ray data. Cyclohexane-based 1,3- dithiolane-2-thiones revealed a trans-fusion of the carbo- and hetero-cycles. The products obtained from the mono-substituted cyclohexene oxides demonstrated an axial position of the substituents. Thus the epoxide transformation into trithiocarbonate can be used as a method for locking cyclic compounds in unstable conformations.ARKAT-USA, Inc.

THE REACTION OF FIVE-MEMBERED CYCLIC TRITHIOCARBONATES WITH n-BUTYLLITHIUM

It was found that the reaction of five-membered cyclic trithiocarbonates with n-butylithium in tetrahydrofuran is applicable to the preparation of unsymmetrical linear trithiocarbonates and further to the interconversion of cis- and trans olefins.