521984-94-1Relevant articles and documents
Synthesis of pyrrolo-heterocycles via Pd-loaded zeolite catalyzed annulation of o- haloaromatic amine with terminal alkynes
Yum, Eul Kgun,Hong, Ki Bum
, p. 6581 - 6586 (2017)
A Pd-loaded zeolite-catalyzed heteroannulation of various 2-iodopyridines and 2-iodoquinolines with terminal alkyne is demonstrated. This approach provides a rapid and convergent synthesis toward a diverse range of pyrrolo-pyridines (azaindoles) and pyrrolo-quinoline ring systems. The Pd-zeolite catalyst can be reused within the same reaction without reactivation of the Pd-zeolite catalyst. Furthermore, Pd-zeolite catalysis is an interesting alternative to homogeneous catalysis for the synthesis of heterocycles.
Direct C-H bond activation: Palladium-on-carbon as a reusable heterogeneous catalyst for C-2 arylation of indoles with arylboronic acids
Bhattacharjee, Prantika,Bora, Utpal,Boruah, Purna K.,Das, Manash R.
, p. 7675 - 7682 (2020/06/09)
Direct C(sp2)-H bond functionalization of indoles with arylboronic acids is achieved using palladium supported on carbon as a reusable heterogeneous catalyst in the presence of an oxidant under mild conditions. The current protocol formed exclusive C-2 selective products without the aid of any ligand or directing group. The catalyst is reusable for up to four catalytic cycles with the retention of catalytic efficiency.
Palladium-catalyzed regioselective C-2 arylation of 7-azaindoles, indoles, and pyrroles with arenes
Laha, Joydev K.,Bhimpuria, Rohan A.,Prajapati, Dilip V.,Dayal, Neetu,Sharma, Shubhra
supporting information, p. 4329 - 4332 (2016/03/22)
A palladium-catalyzed regioselective C-2 arylation of 7-azaindoles, indoles, and pyrroles with arenes has been developed. This study unveils that a critical substrate dependent acid concentration is essential for achieving exclusive C-2 selectivity as wel