Progress in heterocyclic chemistry, Journal Year: 2023, Volume and Issue: unknown, P. 387 - 424
Published: Jan. 1, 2023
Language: Английский
Progress in heterocyclic chemistry, Journal Year: 2023, Volume and Issue: unknown, P. 387 - 424
Published: Jan. 1, 2023
Language: Английский
Organic & Biomolecular Chemistry, Journal Year: 2021, Volume and Issue: 19(38), P. 8184 - 8204
Published: Jan. 1, 2021
The present review is focused on recent advances (2015–present) in the synthesis of 2,4,6-triarylpyridines (also known as Kröhnke pyridines).
Language: Английский
Citations
17RSC Advances, Journal Year: 2022, Volume and Issue: 12(13), P. 8263 - 8273
Published: Jan. 1, 2022
An efficient protocol for the preparation of pyridine skeletons has been successfully developed involving TMSOTf/HMDS (trifluoromethanesulfonic acid/hexamethyldisilane) system intermolecular cyclization chalcones under MW (microwave) irradiation conditions. This method provides a facile approach to synthesize 2,4,6-triaryl or 3-benzyl-2,4,6-triarylpyridines in good excellent yields. Interestingly, 2,6-diazabicyclo[2.2.2]oct-2-ene core was obtained by changing acid additive Sn(OTf)2, and desired product also confirmed using X-ray single-crystal diffraction analysis.
Language: Английский
Citations
9ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(12)
Published: March 25, 2024
Abstract An efficient TBHP/TBAI mediated strategy has been developed for the synthesis of 2,4,6‐trisubstitued pyridines from ketoxime acetates and benzylamines under metal‐free conditions first time. In this protocol benzylamine acts as an effective ArCO surrogate. This methodology features use inexpensive catalysts, avert additional ligands additives high functional group tolerance. Moreover, 5‐Lipoxygenase enzyme inhibitory activities were performed all synthesised compounds. Among 2,4,6‐trisubstituted 3fg, 3fa 3eg showed good activity.
Language: Английский
Citations
1ACS Omega, Journal Year: 2022, Volume and Issue: 7(31), P. 27157 - 27163
Published: July 27, 2022
A simple and efficient protocol has been developed to access symmetrical unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles from arylacetic acids hydrazides via copper-catalyzed dual oxidation under an oxygen atmosphere. Oxidative decarboxylation of oxidative functionalization the imine C–H bond are key steps. This is first example synthesis through in one-pot. Avoidance expensive ligand high yield products advantageous features method.
Language: Английский
Citations
6Chemistry - An Asian Journal, Journal Year: 2022, Volume and Issue: 18(1)
Published: Dec. 3, 2022
A direct access to unsymmetrical and symmetrical multi-substituted pyridines has been accomplished via iron-catalysed [3+3] annulation of oxime acetates with enaminones. This protocol is featured by easily available starting materials, no requirement expensive additives ligands, operational simplicity, good tolerance diverse functional groups.
Language: Английский
Citations
6Materials Today Chemistry, Journal Year: 2022, Volume and Issue: 25, P. 100971 - 100971
Published: June 2, 2022
Language: Английский
Citations
5The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(18), P. 12957 - 12966
Published: Aug. 28, 2024
A facile one pot sequential and highly chemoselective synthesis of substituted pyridines/pyrido[3,2-
Language: Английский
Citations
0Progress in heterocyclic chemistry, Journal Year: 2023, Volume and Issue: unknown, P. 387 - 424
Published: Jan. 1, 2023
Language: Английский
Citations
0