Palladium-catalyzed carbonylative cyclization of Baylis–Hillman adducts. An efficient approach for the stereoselective synthesis of 3-alkenyl phthalides
F Coelho, D Veronese, CH Pavam, VI de Paula…
Index: Coelho, Fernando; Veronese, Demetrius; Pavam, Cesar H.; de Paula, Vanderlei I.; Buffon, Regina Tetrahedron, 2006 , vol. 62, # 18 p. 4563 - 4572
Full Text: HTML
Citation Number: 53
Abstract
A palladium-mediated carbonylative cyclization reaction of Baylis–Hillman adducts is disclosed. This simple, efficient and straightforward sequence leads to the formation of an array of 3-alkenylphthalides with different substitution patterns on the aromatic ring, with good chemical yields and selectivities.
Related Articles:
Axially Chiral Binaphthyl Surrogates with an Inner N− H− N Hydrogen Bond
[Kawabata, Takeo; Jiang, Changsheng; Hayashi, Kazuhiro; Tsubaki, Kazunori; Yoshimura, Tomoyuki; et al. Journal of the American Chemical Society, 2009 , vol. 131, p. 54 - 55]
[Journal of Organic Chemistry, , vol. 76, # 15 p. 6414 - 6420]
[Journal of Organic Chemistry, , vol. 76, # 15 p. 6414 - 6420]