American Chemical Society
Browse
ja103973a_si_001.pdf (6.01 MB)

Iron-Catalyzed Suzuki−Miyaura Coupling of Alkyl Halides

Download (6.01 MB)
journal contribution
posted on 2010-08-11, 00:00 authored by Takuji Hatakeyama, Toru Hashimoto, Yoshiyuki Kondo, Yuichi Fujiwara, Hirofumi Seike, Hikaru Takaya, Yoshinori Tamada, Teruo Ono, Masaharu Nakamura
In the presence of novel iron(II) chloride−diphosphine complexes and magnesium bromide, lithium arylborates react with primary and secondary alkyl halides to give the corresponding coupling products in good to excellent yields. High functional group compatibility is also demonstrated in the reactions of substrates possessing reactive substituents, such as alkoxycarbonyl, cyano, and carbonyl groups.

History