S Asghar, SB Tailor, D Elorriaga… - Angewandte …, 2017 - Wiley Online Library
Readily accessed cobalt pre‐catalysts with N‐heterocyclic carbene ligands catalyze the Suzuki cross‐coupling of aryl chlorides and bromides with alkyllithium‐activated arylboronic …
J Shi, J Zhou, Y Yan, J Jia, X Liu, H Song… - Chemical …, 2015 - pubs.rsc.org
Here a new, mild and versatile method for one-pot cascade synthesis of diverse N- methoxyisoquinolinediones via Rh (III)-catalyzed regioselective carbenoid insertion C–H …
CF Liu, M Liu, L Dong - The Journal of Organic Chemistry, 2018 - ACS Publications
A highly efficient iridium-catalyzed cascade annulation of pyrazolones and sulfoxonium ylides to access various pyrazolo [1, 2-α] cinnoline derivatives has been achieved. This …
X Mao, J Ni, B Xu, C Ding - Organic Chemistry Frontiers, 2020 - pubs.rsc.org
A facile and efficient approach for the direct thiocyanation of pyrazolin-5-ones via a radical mechanism has been established for the first time. A series of 4-thiocyanated 5-hydroxy-1H …
Salicylic acids are shown to be readily available and versatile starting materials that easily undergo a tandem arylation–protodecarboxylation process under Pd-catalysis. The …
VB Purohit, RV Prajapati, VD Prajapati… - European Journal of …, 2022 - Wiley Online Library
In this contribution, we provide a comprehensive overview on the C− H activation/ functionalization reactions of 1‐aryl‐5‐pyrazolones, in particular, 1‐aryl‐3‐methyl‐1H …
P Li, X Xu, J Chen, H Yao, A Lin - Organic Chemistry Frontiers, 2018 - pubs.rsc.org
Rhodium (III)-catalyzed redox-neutral annulation of pyrazolidinones with diazo compounds has been described. This reaction provides a straightforward platform to access various …
S Mayakrishnan, Y Arun, C Balachandran… - Organic & …, 2016 - pubs.rsc.org
Rhodium catalysed dehydrogenative C–H/N–H functionalization was developed to construct phthalazino [2, 3-a]-/indazolo [1, 2-a] cinnolines by reacting N-phenyl phthalazine/indazole …
Herein, a straightforward synthetic approach for the construction of phenanthridin-6 (5 H)- one skeletons is disclosed. The developed protocol relies on palladium catalysis, providing …