Palladium nanoparticle catalysis: borylation of aryl and benzyl halides and one-pot biaryl synthesis via sequential borylation-Suzuki–Miyaura coupling
A Bej, D Srimani, A Sarkar
Index: Bej, Ansuman; Srimani, Dipankar; Sarkar, Amitabha Green Chemistry, 2012 , vol. 14, # 3 p. 661 - 667
Full Text: HTML
Citation Number: 27
Abstract
Palladium nanoparticles generated in PEG catalyze the reaction of bis (pinacolato) diboron with various aryl/benzyl halides to afford aryl/benzyl boronates in high yield. Arylboronates thus prepared, have been directly used in the Suzuki–Miyaura coupling reaction with different aryl halides and benzyl halides in a convenient one-pot, two-step solvent free green synthesis of unsymmetrical biaryls and diarylmethanes.
Related Articles:
[Ratniyom, Jadsada; Dechnarong, Nattanee; Yotphan, Sirilata; Kiatisevi, Supavadee European Journal of Organic Chemistry, 2014 , vol. 2014, # 7 p. 1381 - 1385]
[Broutin, Pierre-Emmanuel; Cerna, Igor; Campaniello, Maria; Leroux, Frederic; Colobert, Francoise Organic Letters, 2004 , vol. 6, # 24 p. 4419 - 4422]
[Wang, Lianhui; Li, Jingya; Cui, Xiuling; Wu, Yusheng; Zhu, Zhiwu; Wu, Yangjie Advanced Synthesis and Catalysis, 2010 , vol. 352, # 11-12 p. 2002 - 2010]
[Melaimi, Mohand; Thoumazet, Claire; Ricard, Louis; Le Floch, Pascal Journal of Organometallic Chemistry, 2004 , vol. 689, # 19 p. 2988 - 2994]
[Murata, Miki; Sambommatsu, Tomoko; Watanabe, Shinji; Masuda, Yuzuru Synlett, 2006 , # 12 p. 1867 - 1870]