99842-48-5Relevant articles and documents
An organophotoredox-catalyzed redox-neutral cascade involving: N -(acyloxy)phthalimides and allenamides: Synthesis of indoles
Das, Sanju,Azim, Aznur,Hota, Sudhir Kumar,Panda, Satya Prakash,Murarka, Sandip,De Sarkar, Suman
supporting information, p. 13130 - 13133 (2021/12/16)
An organophotoredox-catalyzed radical cascade of allenamides and alkyl N-(acyloxy)phthalimides for the synthesis of indoles is documented. The method features mild and robust reaction conditions, and exhibits broad scope. The tandem process enriches the l
Transition-Metal-Free Stereoselective Borylation of Allenamides
García, Lorena,Sendra, Jana,Miralles, Núria,Reyes, Efraim,Carbó, Jorge J.,Vicario, Jose L.,Fernández, Elena
supporting information, p. 14059 - 14063 (2018/09/10)
Complete stereocontrol on the transition-metal-free hydroboration of the distal double bond of allenamides could be achieved when allenamides contained acetyl substituents, which provided exclusively the Z-isomer. The consecutive Pd-catalyzed cross-coupli
Selective cleavage of the N-propargyl group from sulfonamides and amides under ruthenium catalysis
Wang, Jingjing,Li, Feng,Pei, Wenlong,Yang, Mixue,Wu, Yidan,Ma, Danyang,Zhang, Furong,Wang, Jianhui
supporting information, p. 1902 - 1905 (2018/04/19)
The selective cleavage of the N-propargyl group from sulfonamides and amides under ruthenium catalysis is described. The reaction tolerates a broad range of functional groups, and the desired products were obtained in 10–95% yield.
