295324-71-9

Upstream product

• 98078-15-0 6-phenylhex-5-en-1-ol 
• 100-52-7 benzaldehyde 
• 34626-52-3 5-hydroxypentyltriphenylphosphonium bromide 
• 111-24-0 1,5-dibromo-pentane 

Downstream Products

• 1330074-89-9 C₂₁H₂₀ClNO 
• 1352632-22-4 C₂₁H₂₀ClNO 
• 3900-93-4 2-cyclopentyl-2-phenylacetic acid 
• 58007-86-6 C₂₄H₃₀ 
• 6111-82-6 1-phenylhex-1-ene 

Relevant academic research and scientific papers

Studies on the Wittig reaction (XXX): Stereoselective synthesis and bioactivity of 1-aryl-6-(1,2,4-triazol-1-yl)-1-hexenes

Twelve 1-aryl-6-(1,2,4-triazol-1-yl)-1-hexenes 4 were synthesized by N-alkylation of alkenyl bromides 3, which were obtained by the Wittig reaction of 5-hydroxypentyltriphenylphosphonium bromide 1 with various aromatic aldehydes and subsequent bromination

One-pot synthesis of fused benzo[c]carbazoles by photochemical intramolecular annulation of 3-acyl-2-haloindoles with tethered styrenes

An efficient procedure for the synthesis of fused benzo[c]carbazoles has been achieved in moderate to high yields by the one-pot photochemical annulation of 3-acyl-2-haloindoles with tethered styrenes by photoinduced electron-transfer coupling, electrocyclic reactions, and deacylative aromatization in the presence of pyridine. Fused furo[2,3-c]carbazoles were also synthesized under the same conditions. 5,6-Dihydrobenzo[c]pyrrolo[1,2,3-lm] carbazoles were oxidized by DDQ to afford aromatic benzo[c]pyrrolo[1,2,3-lm] carbazole products in moderate to high yields.

One-pot synthesis of benzo[f]quinolin-3-ones and benzo[a]phenanthridein-5- ones by the photoanuulation of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1- ones to phenylacetylene

The one-pot synthesis of benzo[f]quinolin-3-ones and benzo[a] phenanthridein-5-ones was achieved by the inter- and intramolecular photoannulation of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1-ones with phenylacetylene or tethered phenylacetylene. The reactions were proceeded by photoaddition of 6-chloropyridin-2-ones and 3-chloroisoquinolin-1-ones to phenylacetylene to give the chlorine-substituted stilbenoids, and then 6π electrocyclization of the stilbenoids and oxidation aromatization to afford the polycyclic products.