Facile Synthesis of Acridine Derivatives by ZnCl2-Promoted Intramolecular Cyclization of o-Arylaminophenyl Schiff Bases
Q Su, P Li, M He, Q Wu, L Ye, Y Mu
Index: Su, Qing; Li, Pei; He, Mina; Wu, Qiaolin; Ye, Ling; Mu, Ying Organic Letters, 2014 , vol. 16, # 1 p. 18 - 21
Full Text: HTML
Citation Number: 10
Abstract
A concise and efficient method for the synthesis of a wide range of acridine derivatives and polycyclic aza-aromatic compounds from a ZnCl2-promoted cyclization reaction of readily available o-arylaminophenyl Schiff base compounds under convenient conditions was developed. Reaction conditions and scope of the new method were examined in detail.
Related Articles:
[Colter, Allan K.; Plank, Peter; Bergsma, John P.; Lahti, Roy; Quesnel, Andre A.; Parsons, Gregg Canadian Journal of Chemistry, 1984 , vol. 62, p. 1780 - 1784]
Nickel-catalyzed transformations of 2, 1-benzisoxazoles with organozinc reagents
[Baum, Jonathan S.; Condon, Michael E.; Shook, David A. Journal of Organic Chemistry, 1987 , vol. 52, # 14 p. 2983 - 2988]
[Colter, Allan K.; Plank, Peter; Bergsma, John P.; Lahti, Roy; Quesnel, Andre A.; Parsons, Gregg Canadian Journal of Chemistry, 1984 , vol. 62, p. 1780 - 1784]
[Colter, Allan K.; Plank, Peter; Bergsma, John P.; Lahti, Roy; Quesnel, Andre A.; Parsons, Gregg Canadian Journal of Chemistry, 1984 , vol. 62, p. 1780 - 1784]