85352-32-5

Upstream product

• 6302-93-8 5-[Bis(phenylsulfanyl)methyl]-1,3-benzodioxole 
• 592-04-1 mercury(II) cyanide 
• 120-57-0 piperonal 
• 882-33-7 diphenyldisulfane 
• 4439-02-5 3,4-methylenedioxyphenylacetonitrile 

Downstream Products

• 129819-59-6 N-2-(2-furylethyl) α-phenylthio-1,3-benzodioxole-5-ethanamine 
• 129819-55-2 N-3,5-hexadienyl α-phenylthio-1,3-benzodioxole-5-ethanamine 
• 129819-62-1 (2-Benzo[1,3]dioxol-5-yl-2-phenylsulfanyl-ethyl)-(2-furan-2-yl-ethyl)-carbamic acid ethyl ester 
• 129819-56-3 (2-Benzo[1,3]dioxol-5-yl-2-phenylsulfanyl-ethyl)-((E)-hexa-3,5-dienyl)-carbamic acid ethyl ester 
• 129819-57-4 ethyl <2-(1,3-benzodioxol-5-yl)-2-phenylthioethyl>methylcarbamate 
• 129819-51-8 ethyl 2-(1,3-benzodioxol-5-yl)-2-phenylthioethylcarbamate 
• 126798-87-6 α-phenylthio-1,3-benzodioxoleacetaldehyde 
• 85352-33-6 4-Benzo[1,3]dioxol-5-yl-4-cyano-4-phenylsulfanyl-butyric acid ethyl ester 
• 129819-50-7 α-phenylthio-1,3-benzodioxole-5-ethanamine 

Relevant academic research and scientific papers

PREPARATION OF N-ALKADIENYL N-E-2-ARYLETHENYLCARBAMATES VIA SULFOXIDE ELIMINATION IN A SYNTHETIC APPROACH TO LYCORINE

N-E-2-Arylethenylcarbamates have been prepared in good yields from N-carbamates via sulfoxide elimination towards nitrogen.

NOVEL CONFORMATIONAL EFFECTS OF THE N-BENZYLOXYCARBONYL-CIS-3a-ARYL-OCTAHYDROINDOLE NUCLEUS. FORMAL TOTAL SYNTHESIS OF RACEMIC ELWESINE AND EPIELWESINE

The formal total synthesis of racemic elwesine (I) and epielwesine (II) is described.The preferred ground-state conformation of the cis-3a-aryl-octahydroindole precursors is shown to be dependent on the substituent on nitrogen.