1352656-24-6Relevant articles and documents
Pd-catalyzed regioselective and stereospecific Suzuki-Miyaura coupling of allylic carbonates with arylboronic acids
Li, Chenguang,Xing, Juxiang,Zhao, Jingming,Huynh, Patrick,Zhang, Wanbin,Jiang, Pingkai,Zhang, Yong Jian
supporting information; experimental part, p. 390 - 393 (2012/02/15)
The Pd-catalyzed Suzuki-Miyaura coupling reaction of unsymmetric 1,3-disubstituted secondary allylic carbonates with arylboronic acids has been developed in a wet solvent under a base-free system to afford allyl-aryl coupling products in a high level of isolated yields with complete regio- and E/Z-selectivities with good to excellent chemoselectivities. The coupling reaction of optically active allyl carbonates gave allyl-aryl coupling products with excellent enantioselectivities with inversion of the stereochemistry. This coupling method was successfully applied to the synthesis of (S)-naproxen.