1334484-52-4

Upstream product

• 1822-73-7 phenylthioethylene 
• 1513-65-1 2,6-difluoro pyridine 
• 1334484-51-3 C₁₂H₁₄OS 

Downstream Products

• 1334484-25-1 2-fluoro-6-(1-cyclopropyl-2-(phenylsulfonyl)allyloxy)pyridine 
• 1334484-34-2 (E)-3-(3-cyclopropyl-2-(phenylsulfonyl)allyl)dihydrofuran-2(3H)-one 
• 1334484-35-3 (E)-6-cyclopropyl-1,1-dimethoxy-5-(phenylsulfonyl)hex-5-en-2-one 
• 1334484-36-4 (E)-1-cyclopropyl-6,6-dimethyl-8-oxo-2-(phenylsulfonyl)non-1-en-4-yl pivalate 
• 1334484-44-4 (8S,9S,10R,13S,14S,17R)-17-((E)-5-cyclopropyl-4-(phenylsulfonyl)pent-4-enoyl)-17-hydroxy-10,13-dimethyl-7,8,9,10,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,11(2H,6H)-dione 

Relevant academic research and scientific papers

Tri- and tetrasubstituted functionalized vinyl sulfides by radical allylation

2-Fluoropyridinyl-6-oxy- precursors derived from phenyl vinyl sulfide react with radicals generated from xanthates via an addition-elimination process to furnish the corresponding vinyl sulfides in good yields. This convergent method is operationally simp

A highly stereoselective, modular route to (E)-vinylsulfones and to (Z)- and (E)-alkenes

A recently discovered radical fragmentation of 2-fluoro-6-pyridinoxy derivatives allows a new highly stereoselective and convergent route to (E)-vinylsulfones from allylic alcohols. Reductive desulfonylation or nickel-catalyzed couplings furnish di- and t