Department of Chemistry, Wroclaw University , F. Joliot-Curie 14, Wroclaw 50-383, Poland.
Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
J Org Chem. 2016 Sep 2;81(17):8091-4. doi: 10.1021/acs.joc.6b01560. Epub 2016 Aug 2.
Amide N-C(O) bonds are generally unreactive in cross-coupling reactions employing low-valent transition metals due to nN → π*C═O resonance. Herein we demonstrate that N-acyl-tert-butyl-carbamates (Boc) and N-acyl-tosylamides (Ts), two classes of acyclic amides that have recently enabled the development of elusive amide bond N-C cross-coupling reactions with organometallic reagents, are intrinsically twisted around the N-C(O) axis. The data have important implications for the design of new amide cross-coupling reactions with the N-C(O) amide bond cleavage as a key step.
酰胺 N-C(O) 键在使用低价过渡金属的交叉偶联反应中通常是不反应的,这是由于 nN → π*C═O 共振。在此,我们证明 N-酰基叔丁基氨基甲酸酯(Boc)和 N-酰基对甲苯磺酰胺(Ts),这两类无环酰胺最近使得与有机金属试剂进行难以捉摸的酰胺键 N-C 交叉偶联反应的发展成为可能,它们在 N-C(O) 轴周围是固有扭曲的。这些数据对设计新的酰胺交叉偶联反应具有重要意义,其中 N-C(O) 酰胺键的断裂是关键步骤。