Uses of K2S2O8 in Metal-Catalyzed and Metal-Free Oxidative Transformations

S Mandal, T Bera, G Dubey, J Saha, JK Laha - ACS Catalysis, 2018 - ACS Publications
Carbon–carbon/carbon–heteroatom bond formation via oxidative transformations is a
heavily explored topic at the frontier of chemistry. Potassium persulfate (K2S2O8) has …

Cobalt‐Catalyzed Suzuki Biaryl Coupling of Aryl Halides

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 …

One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh (iii)-catalyzed carbenoid insertion C–H activation/cyclization

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 …

Iridium (III)-catalyzed tandem annulation synthesis of pyrazolo [1, 2-α] cinnolines from pyrazolones and sulfoxonium ylides

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 …

K 2 S 2 O 8-promoted direct thiocyanation of pyrazolin-5-ones with ammonium thiocyanate at room temperature

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 as readily available starting materials for the synthesis of meta-substituted biaryls

J Luo, S Preciado, I Larrosa - Chemical Communications, 2015 - pubs.rsc.org
Salicylic acids are shown to be readily available and versatile starting materials that easily
undergo a tandem arylation–protodecarboxylation process under Pd-catalysis. The …

C− H Functionalization Reactions of 1‐Aryl‐5‐pyrazolones

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 …

Rh (III)-Catalyzed synthesis of pyrazolo [1, 2-a] cinnolines from pyrazolidinones and diazo compounds

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 …

Synthesis of cinnolines via Rh (III)-catalysed dehydrogenative C–H/N–H functionalization: Aggregation induced emission and cell imaging

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 …

Construction of phenanthridinone skeletons through palladium-catalyzed annulation

X Geng, H He, A Shatskiy, EV Stepanova… - The Journal of …, 2023 - ACS Publications
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 …