851763-62-7

Upstream product

• 105797-59-9 n-butyl phenylacetylenic telluride 

Downstream Products

• 851763-80-9 (Z)-1,4-diphenyl-2-butyltelluro-1-buten-3-yne 
• 13343-79-8 (E)-1,4-Diphenylbut-1-en-3-yne 
• 886-65-7 trans,trans-1,4-Diphenyl-1,3-butadiene 

Relevant academic research and scientific papers

Hydrozirconation of acetylenic chalcogenides. Synthesis and reactions of zirconated vinyl chalcogenide intermediates

Acetylenic tellurides react with Cp2Zr(H)Cl in THF at room temperature to give the α-zirconated vinyl telluride intermediates 39, which react with a wide range of electrophiles to give several types of trisubstituted olefins, such as α-halo vin

Stereoselective synthesis of 1,3-enynyltellurides via palladium catalysed cross-coupling reaction of (E)-α-iodovinyltellurides

(E)-α-Iodovinyltellurides undergo a direct coupling reaction with terminal alkynes in the presence of [Pd(PPh3)4] and CuI catalysts in pyrrolidine at room temperature to give 1,3-enynyltellurides in good yields.