Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Monoranjan Ghosh"'
Publikováno v:
Organic & Biomolecular Chemistry. 14:1432-1436
A regioselective copper-catalyzed ethoxycarbonyl-difluoromethylation of imidazo[1,2-a]pyridines has been developed through sp(2) C-H bond functionalization with BrCF2CO2Et under ambient air. A series of ethoxycarbonyldifluoromethylated imidazo[1,2-a]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ec900beacb1965c60acd4bade6452f
https://doi.org/10.1039/c5ob02363g
https://doi.org/10.1039/c5ob02363g
Autor:
Monoranjan Ghosh, Alakananda Hajra
Publikováno v:
European Journal of Organic Chemistry. 2015:7836-7841
A DABCO-promoted intermolecular cyclization between enols and nitrostyrenes has been developed for the regioselective synthesis of angularly fused furan derivatives in high yields. This protocol is applicable to various enol derivatives, including 4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce55f1e75f0851b9a0ae657caa3c728b
https://doi.org/10.1002/ejoc.201501152
https://doi.org/10.1002/ejoc.201501152
Publikováno v:
Chemistry - An Asian Journal. 10:2525-2536
A versatile method for the diversified synthesis of furans and arenofurans has been developed that proceeds through K2CO3-promoted cyclization between enols/1,3-dicarbonyl compounds and nitroolefins at reflux in EtOH. This facile method has been succ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dfabb351a835dbbc9a9ae3a51aef510
https://doi.org/10.1002/asia.201500710
https://doi.org/10.1002/asia.201500710
Publikováno v:
Tetrahedron Letters. 56:4101-4104
Palladium-catalyzed direct dehydrogenative annulation of imidazo[1,2-a]pyridines with diarylalkynes through dual cleavage of C–H bonds has been developed. This new strategy offers a straightforward route for the synthesis of π-conjugated polyaroma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b48d26e68a1f3af2216ec490f52e0224
https://doi.org/10.1016/j.tetlet.2015.05.028
https://doi.org/10.1016/j.tetlet.2015.05.028
Publikováno v:
The Journal of Organic Chemistry. 80:5364-5368
A copper-mediated intermolecular annulation of alkyl ketones and β-nitrostyrenes has been developed for the regioselective synthesis of multisubstituted furan derivatives in good yields. This protocol is applicable to both cyclic and acyclic ketones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f315339e835434ecc5479756879a990e
https://doi.org/10.1021/acs.joc.5b00704
https://doi.org/10.1021/acs.joc.5b00704
Publikováno v:
Organic & Biomolecular Chemistry. 13:8717-8722
A simple and practical method has been developed for the regioselective nitrosylation of imidazopyridines via C(sp(2))-H bond functionalization using tert-butyl nitrite under mild reaction conditions in a short time. A library of 3-nitrosoimidazopyri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05b8658dca1f67e2cb40fb13ee75e8f2
https://doi.org/10.1039/c5ob01345c
https://doi.org/10.1039/c5ob01345c
Publikováno v:
Tetrahedron Letters. 55:235-239
Benzoquinazolin-2-one derivatives were synthesized by using a catalytic amount of task specific ionic liquid, [1-methyl-3-(4-sulfobutyl)imidazolium-4-methylbenzenesulfonate] through a one-pot multicomponent Biginelli reaction of α-tetralone, aldehyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7521d881f10edb0af783414b90a981
https://doi.org/10.1016/j.tetlet.2013.11.011
https://doi.org/10.1016/j.tetlet.2013.11.011
Publikováno v:
European Journal of Organic Chemistry. 2014:1096-1102
An efficient and environmentally benign method has been developed for the synthesis of symmetrical and unsymmetrical aromatic azo compounds through phenyliodine(III) diacetate (PIDA) mediated oxidative dehydrogenative coupling of anilines in high yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9772f65e6ff09e8c39102a6c0f6d6247
https://doi.org/10.1002/ejoc.201301209
https://doi.org/10.1002/ejoc.201301209
Publikováno v:
ChemInform. 47
A regioselective copper-catalyzed ethoxycarbonyl-difluoromethylation of imidazo[1,2-a]pyridines has been developed through sp2 C–H bond functionalization with BrCF2CO2Et under ambient air. A series of ethoxycarbonyldifluoromethylated imidazo[1,2-a]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb721d168e0ac5c3fdd7a917804c4440
https://doi.org/10.1002/chin.201622167
https://doi.org/10.1002/chin.201622167
Autor:
Alakananda Hajra, Monoranjan Ghosh
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8358acdc7ce108f28f9f3aafa53239f
https://doi.org/10.1002/chin.201615035
https://doi.org/10.1002/chin.201615035