Iodine-promoted sequential C (sp 3)–H oxidation and cyclization of aryl methyl ketones with 2-(2-aminophenyl) quinazolin-4 (3 H)-ones

M Arockiaraj, V Rajeshkumar - Organic & Biomolecular Chemistry, 2024 - pubs.rsc.org
An I2-promoted, metal-free protocol has been developed for the one-pot synthesis of 6-aroyl-
5, 6-dihydro-8H-quinazolino [4, 3-b] quinazolin-8-ones from readily accessible substrates …

I2-Cs2CO3 Mediated Intramolecular C2-Amination and Oxidative Rearrangement Cascade of C-3 Phenylthio Indoles: A Route to Synthesize Thiosulfonate …

G Singh, SS Marupalli, M Arockiaraj… - The Journal of …, 2024 - ACS Publications
An efficient, transition-metal-free protocol employing I2/Cs2CO3 for the synthesis of
thiosulfonate containing 2-iminoindolin-3-ones motifs has been developed from C-3 …

Base-promoted fused β-carboline formation from 2-(1 H-indol-3-yl) cyclohexan-1-ones, aldehydes and ammonium salts

J Chen, Y Zhang, X Liu, K Liu, J Wu, X Peng… - Organic Chemistry …, 2024 - pubs.rsc.org
A novel base-promoted fused β-carboline formation strategy from 2-(1H-indol-3-yl)
cyclohexan-1-ones, aldehydes and ammonium salts has been developed. In this cascade …

I 2-catalyzed tandem sp 3 C–H oxidation and annulation of aryl methyl ketones with amidoximes for the synthesis of 5-aroyl-1, 2, 4-oxadiazoles

SK Punna, M Arockiaraj, V Rajeshkumar - Organic & Biomolecular …, 2024 - pubs.rsc.org
A metal-free, iodine-catalyzed protocol has been developed for constructing biologically
significant 5-aroyl 1, 2, 4-oxadiazole scaffolds using aryl methyl ketones and amidoximes …

I2‐Promoted sp3 C–H Oxidation/Annulation Sequences for the Synthesis of Indoloquinolines from 2‐(1H‐indol‐2‐yl) anilines and Aryl Methyl Ketones

M Arockiaraj, V Rajeshkumar - Advanced Synthesis & Catalysis, 2024 - Wiley Online Library
An iodine/DMSO‐promoted metal‐free approach has been developed for the synthesis of
indoloquinolines via a sequential sp3 C‐H oxidation/intramolecular cyclization using 2‐(1H …

[引用][C] Reduction of C= X to CH2

P Adler - 2024 - Elsevier