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.