Recent advances in the use of dimethyl sulfoxide as a synthon in organic chemistry
H Lu, Z Tong, L Peng, Z Wang, SF Yin… - Topics in Current …, 2022 - Springer
Dimethyl sulfoxide (DMSO), as extremely important aprotic polar solvent and reaction
medium, has attracted widespread attention from chemists in recent years due to its wide …
medium, has attracted widespread attention from chemists in recent years due to its wide …
The recent advances in K 2 S 2 O 8-mediated cyclization/coupling reactions via an oxidative transformation
S Kumar, K Padala - Chemical Communications, 2020 - pubs.rsc.org
Transition metal-free organic transformations using K2S2O8 is one of the most efficient
methods for the formation of carbon–carbon/carbon–heteroatom bond in organic synthesis …
methods for the formation of carbon–carbon/carbon–heteroatom bond in organic synthesis …
Recent advances and prospects in the organocatalytic synthesis of quinazolinones
B Borah, S Swain, M Patat, LR Chowhan - Frontiers in Chemistry, 2022 - frontiersin.org
Quinazolinone, a bicyclic compound, comprises a pyrimidine ring fused at 4´ and 8´
positions with a benzene ring and constitutes a substantial class of nitrogen-containing …
positions with a benzene ring and constitutes a substantial class of nitrogen-containing …
α-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo [1, 2-a] quinoxalines, quinazolinones, and other N-heterocycles via decarboxylative oxidative …
M Viji, M Vishwanath, J Sim, Y Park, C Jung, S Lee… - RSC …, 2020 - pubs.rsc.org
A metal-free and efficient procedure for the synthesis of pyrrolo [1, 2-a] quinoxalines,
quinazolinones, and indolo [1, 2-a] quinoxaline has been developed. The key features of our …
quinazolinones, and indolo [1, 2-a] quinoxaline has been developed. The key features of our …
Hydroxymethylation of active methenyl compounds: DMSO as methylene source and H2O as oxygen source
L Zhang, S Liu, Y Lin, Y Wang - Tetrahedron Letters, 2022 - Elsevier
A mild and efficient method for hydroxymethylation of active methenyl compounds has been
described. In this transformation, the widely available solvents DMSO and H 2 O served as …
described. In this transformation, the widely available solvents DMSO and H 2 O served as …
Electrochemical access to benzimidazolone and quinazolinone derivatives via in situ generation of isocyanates
D Saha, IM Taily, S Naik, P Banerjee - Chemical Communications, 2021 - pubs.rsc.org
Isocyanates are the key intermediates for several organic transformations towards the
synthesis of diverse pharmaceutical targets. Herein, we report the development of an …
synthesis of diverse pharmaceutical targets. Herein, we report the development of an …
H2O2-Mediated Synthesis of a Quinazolin-4(3H)-one Scaffold: A Sustainable Approach
S Kumar, K Padala, B Maiti - ACS omega, 2023 - ACS Publications
A quinazolin-4 (3 H)-one ring system is a privileged heterocyclic moiety with distinctive
biological properties. From this perspective, the development of an efficient strategy for the …
biological properties. From this perspective, the development of an efficient strategy for the …
Reagent-free intramolecular hydrofunctionalization: A regioselective 6-endo-dig cyclization of o-alkynoylphenols
C Jung, S Li, K Lee, M Viji, H Lee, S Hyun, K Lee… - Green …, 2022 - pubs.rsc.org
Solvent-directed intramolecular hydrofunctionalization of readily available o-
alkynoylphenols 1 was successfully achieved under reagent-free conditions. The …
alkynoylphenols 1 was successfully achieved under reagent-free conditions. The …
Metal‐Free, Photoredox‐Catalyzed Synthesis of Quinazolin‐4(3H)‐ones and Benzo[4,5]imidazo[1,2‐c]quinazolines Using Trialkylamines as Alkyl Synthon
A Arumugam, P Palani, M Anandan… - European Journal of …, 2023 - Wiley Online Library
Abstract Highly functionalized quinazolin‐4 (3H)‐ones were synthesized from reactions of N‐
aryl‐2‐aminobenzamides with trialkylamines under photocatalytic conditions by using eosin …
aryl‐2‐aminobenzamides with trialkylamines under photocatalytic conditions by using eosin …
DMSO as a dual carbon synthon in one-pot tandem synthesis of N-alkylated quinazolinones from anthranilamides and acetophenones
P Yadav, S Yadav, A Awasthi, M Phanindrudu… - New Journal of …, 2022 - pubs.rsc.org
A new, efficient, metal-free, and DMSO-assisted approach for the synthesis of N-alkylated
quinazolinones from readily available 2-aminobenzamide and aryl methyl ketones in the …
quinazolinones from readily available 2-aminobenzamide and aryl methyl ketones in the …