TY - JOUR
AU1 - Hu, Ziwei
AU2 - Wang, Jian
AU3 - Liang, Dongdong
AU4 - Zhu, Qiang
AB - A three‐component reaction involving isocyanides, o‐alkynyltrifluoroacetanilides, and amines for the efficient synthesis of 2‐substituted 1H‐indole‐3‐carboxamidines has been developed. The reaction proceeds through intramolecular aminopalladation of alkynes activated by isocyanide‐ligated palladium(II) species. Dioxygen acts as the sole oxidant to regenerate the active palladium(II) species.
TI - Synthesis of 1 H ‐Indole‐3‐carboxamidines through a Palladium‐Catalyzed Three‐Component Reaction Involving Isocyanide Insertion as a Key Step
JF - Advanced Synthesis & Catalysis
DO - 10.1002/adsc.201300532
DA - 2013-11-11
UR - https://www.deepdyve.com/lp/wiley/synthesis-of-1-h-indole-3-carboxamidines-through-a-palladium-catalyzed-XcpWAZhdQv
SP - 3290
EP - 3294
VL - 355
IS - 16
DP - DeepDyve
ER -