66294-44-8Relevant articles and documents
Photoredox/nickel dual-catalyzed regioselective alkylation of propargylic carbonates for trisubstituted allenes
Zhou, Zhao-Zhao,Song, Xian-Rong,Du, Sha,Xia, Ke-Jian,Tian, Wan-Fa,Xiao, Qiang,Liang, Yong-Min
supporting information, p. 9390 - 9393 (2021/09/22)
Herein, a highly regioselective alkylation of propargylic carbonates for trisubstituted allenes with alkyl 1,4-dihydropyridine derivatives (1,4-DHPs) is developedviaa photoredox/nickel dual-catalyzed process, which represents the first direct approach to access alkylated allene products without alkyl organometallic reagents. This method features a broad substrate scope and mild conditions. A hypothetical mechanism with an alkyl radical and an allenyl Ni(iii) species is proposed. Benzylation products were also obtained to be the complement building blocks for the potential synthesis of pharmaceuticals.