Tandem palladium-catalyzed urea arylation-intramolecular ester amidation: regioselective synthesis of 3-alkylated 2, 4-quinazolinediones
MC Willis, RH Snell, AJ Fletcher, RL Woodward
Index: Willis, Michael C.; Snell, Robert H.; Fletcher, Anthony J.; Woodward, Robert L. Organic Letters, 2006 , vol. 8, # 22 p. 5089 - 5091
Full Text: HTML
Citation Number: 57
Abstract
o-Halo benzoates can be combined with monoalkyl ureas in a tandem palladium-catalyzed arylation-ester amidation sequence to deliver quinazolinedione products. The reactions are regioselective for formation of the 3-N-alkyl isomers. Significant variation of both coupling partners is possible, allowing the synthesis of a diverse array of substituted quinazolinediones, exemplified by the preparation of a simple unsymmetric-dialkylated ...
Related Articles:
[Molina, Pedro; Alajarin, Mateo; Vidal, Angel Tetrahedron, 1989 , vol. 45, # 13 p. 4263 - 4286]
[Lee, Hyi-Seung; Chang, Yong-Goo; Kim, Kyongtae Journal of Heterocyclic Chemistry, 1998 , vol. 35, # 3 p. 659 - 668]
[Azizian, Javad; Mohammadi, Ali A.; Karimi, Ali R. Synthetic Communications, 2003 , vol. 33, # 3 p. 415 - 420]
[Journal of Heterocyclic Chemistry, , vol. 35, # 3 p. 659 - 668]
[Tetrahedron, , vol. 45, # 13 p. 4263 - 4286]