19938-95-5

Upstream product

• 21162-22-1 2,6-dimethoxy-4-phenyl-1,2-dihydro-benzo[e][1,2]azaborinine 
• 21162-21-0 1-H-2-pentafluorophenyl-4-phenyl-6-methoxy-1,2-azaboranaphthalene 
• 88001-75-6 C₆F₅BClNH-4-C₆H₄OCH₃ 
• 536-74-3 phenylacetylene 
• 104-94-9 4-methoxy-aniline 
• 19938-96-6 1-phenyl-1-(2-amino-5-methoxyphenyl)ethylene 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Relevant academic research and scientific papers

Acid-Mediated Oxychalcogenation of o-Vinylanilides with N-(Arylthio/arylseleno)succinimides

An efficient acid-mediated oxythiolation of o-vinylanilides has been accomplished, employing N-(arylthio)succinimide as an electrophilic arylthiolating reagent for the synthesis of various arylthio tethered benzoxazine derivatives in good to excellent yie

Palladium(ii)-catalyzed vinylic geminal double C-H activation and alkyne annulation reaction: Synthesis of pentafulvenes

The first transition-metal-catalyzed vinylic geminal double C(sp2)-H activation and di-substituted alkyne annulation reaction is reported. This palladium(ii)-catalyzed, amide directed reaction of vinylic compounds with di-substituted alkynes offers an efficient synthetic path to pentafulvenes, which are very important compounds because of their bioactivity and interesting optical properties. A FeCl3-mediated transformation of pentafulvenes to fluorescent cyclopenta[b]quinolines is also developed.