1428733-72-5Relevant academic research and scientific papers
Expeditious synthesis of aromatic cyanodienones using neutral alumina as a versatile heterogeneous catalyst
Mouradzadegun, Arash,Abadast, Fatemeh
, p. 640 - 647 (2014/01/17)
The work described herein employs neutral alumina as an effective catalyst for ring opening of triarylpyrylium perchlorates to corresponding aromatic cyanodienones, which have main roles in biological activities. The present porous catalyst has several ad
An innovative and atom-efficient synthesis of bioactive 2-aroylfuran derivatives using macroporous polymer-supported cyanide
Mouradzadegun, Arash,Abadast, Fatemeh
supporting information, p. 448 - 452 (2014/03/21)
A novel and safe approach was developed for the synthesis of bioactive 2-aroyl-3,5-diarylfurans in excellent yields by using a cyanide-impregnated anion-exchange resin as a versatile reagent. The possibility of reusing the polymer-supported reagent makes the process environmentally friendly and economically advantageous. Georg Thieme Verlag Stuttgart. New York.
Thermally-induced ring contraction as a novel and straightforward route for the synthesis of 2-furyl acetonitrile derivatives
Mouradzadegun, Arash,Abadast, Fatemeh
supporting information, p. 2641 - 2644 (2013/06/26)
A new, efficient, and simple process has been established for the synthesis of (3,5-diaryl-2-furyl)(aryl)acetonitriles by the reaction of various 2,4,6-triarylpyrylium perchlorates with sodium cyanide.
An improved, safe, and efficient conversion of triarylpyrylium perchlorates to corresponding cyanodienones using Amberlite IRA 910[CN]
Mouradzadegun, Arash,Abadast, Fatemeh
, p. 375 - 379 (2013/05/21)
Triarylpyrylium perchlorates are readily converted into new aromatic cyanodienones by using cyanide impregnated on anion exchange resin as a safe and efficient reagent.
