Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Kasiviswanadharaju Pericherla"'
Publikováno v:
Synthesis. 48:4305-4346
Ytterbium(III) triflate is an efficient and water-tolerant Lewis acid that has been used as a catalyst for a wide range of organic transformations. Various three-, four-, five-, and six-membered, as well as fused, heterocycles have been synthesized u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e6817a0eaab02dd46bcaa26a1e92155
https://doi.org/10.1055/s-0036-1588321
https://doi.org/10.1055/s-0036-1588321
Publikováno v:
Asian Journal of Organic Chemistry. 4:1380-1385
A highly efficient copper-catalyzed one-pot tandem protocol has been developed for the synthesis of naphtho-fused imidazo[1,2-a]pyridines. The transformation involves a Knoevenagel condensation followed by a chemoselective cross-coupling reaction alo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9368307d7706e864df1a89963d634d33
https://doi.org/10.1002/ajoc.201500297
https://doi.org/10.1002/ajoc.201500297
Publikováno v:
Medicinal Chemistry Research. 24:3117-3126
A series of novel piperazine-1,2,3-triazole derivatives, which entailed the bioisosteric replacement of the imidazole moiety and hybridization of two drug scaffolds was prepared by employing the regioselective copper (I)-catalysed azide-alkyne 1,3-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ed88f16cb058fd6a52165598706cd4b
https://doi.org/10.1007/s00044-015-1361-5
https://doi.org/10.1007/s00044-015-1361-5
Publikováno v:
Synthesis. 47:887-912
Advances in the last decade for the synthesis of the imidazo[1,2-a]pyridine scaffold from various substrates employing approaches such as multicomponent reactions, tandem processes, rearrangement reactions, inter- and intramolecular oxidative/reducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ade9d169ab91d5fb3586e69a9085a9c9
https://doi.org/10.1055/s-0034-1380182
https://doi.org/10.1055/s-0034-1380182
Publikováno v:
Tetrahedron Letters. 56:549-553
An efficient and facile protocol has been developed for the synthesis of pyrazolo[1,5-a]pyrimidines through the tandem reaction of 3-aminopyrazoles and chalcones in the presence of catalytic amounts of KOH. The reported method offers access to 5,7-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05fa04545639e5eb0cc491b52c739df9
https://doi.org/10.1016/j.tetlet.2014.11.121
https://doi.org/10.1016/j.tetlet.2014.11.121
Publikováno v:
RSC Advances. 5:3670-3677
A facile synthesis of 3-aroylimidazo[1,2-a]pyridine derivatives has been achieved through the one-pot, three-component tandem reaction of acetophenones, arylaldehydes and 2-aminopyridines in the presence of a catalytic amount of copper(II) chloride a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9d77e63b2cf7f0e36b3d283b63eb523
https://doi.org/10.1039/c4ra13056a
https://doi.org/10.1039/c4ra13056a
Publikováno v:
Tetrahedron. 70:8539-8544
A novel tandem approach has been demonstrated for the direct synthesis of bioactive 3-aroylimidazo[1,2-a]pyridines from chalcones and 2-aminopyridines. The reported tandem reaction is atom-economical and expected to proceed via 1,4-Michael addition f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1506cf8d2cf1f610b04432c59ff40782
https://doi.org/10.1016/j.tet.2014.09.067
https://doi.org/10.1016/j.tet.2014.09.067
Publikováno v:
Synlett. 25:2345-2349
An efficient method has been described for the synthesis of vinyl sulfones via hydrosulfonylation of alkynes using sodium arene sulfinates catalyzed by Cu(OTf)2 under microwave irradiation. A variety of vinyl sulfones was obtained in good to excellen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45a5ec1f039ddaf1da148255f9c0ec46
https://doi.org/10.1055/s-0034-1378546
https://doi.org/10.1055/s-0034-1378546
Publikováno v:
Synlett. 24:2751-2757
A simple and highly efficient protocol for the regioselective synthesis of azole-substituted imidazo[1,2-a]pyridines has been developed using a ligand-free, copper-catalyzed Ullmann-type C–N coupling of 2-(2-bromophenyl)imidazo[1,2-a]pyridines with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb82744d70bcc4b1ceb95171e24a85b0
https://doi.org/10.1055/s-0033-1339927
https://doi.org/10.1055/s-0033-1339927
Publikováno v:
Organic Letters. 15:4304-4307
A ligand-free copper-catalyzed tandem azide-alkyne cycloaddition (CuAAC), Ullmann-type C-N coupling, and intramolecular direct arylation has been described. The designed strategy resulted in the synthesis of a novel trazole-fused azaheterocycle frame
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910992e35fd41cc2daa6a27674784de0
https://doi.org/10.1021/ol401655r
https://doi.org/10.1021/ol401655r