10.1021/ja103973a.s002 Takuji Hatakeyama Takuji Hatakeyama Toru Hashimoto Toru Hashimoto Yoshiyuki Kondo Yoshiyuki Kondo Yuichi Fujiwara Yuichi Fujiwara Hirofumi Seike Hirofumi Seike Hikaru Takaya Hikaru Takaya Yoshinori Tamada Yoshinori Tamada Teruo Ono Teruo Ono Masaharu Nakamura Masaharu Nakamura Iron-Catalyzed Suzuki−Miyaura Coupling of Alkyl Halides American Chemical Society 2010 presence alkyl halides Suzuki reactive substituents Alkyl HalidesIn group compatibility complex magnesium bromide chloride cyano lithium arylborates alkoxycarbonyl substrate yield High carbonyl groups 2010-08-11 00:00:00 Dataset https://acs.figshare.com/articles/dataset/Iron_Catalyzed_Suzuki_Miyaura_Coupling_of_Alkyl_Halides/2743612 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.