Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Jiří Hanusek"'
Autor:
Martin Kocúrik, Pavlína Konopáčová, Lukáš Kolman, Pavel Kryl, Aleš Růžička, Jan Bartáček, Jiří Hanusek, Jiří Váňa
Publikováno v:
ACS Omega, Vol 9, Iss 47, Pp 47105-47113 (2024)
Externí odkaz:
https://doaj.org/article/82972853f5bb44a88553ebef07141630
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 808-819 (2023)
Reactions of thiobenzamide or thioacetamide with 4-bromo-1,1-dimethyl-1,4-dihydroisoquinoline-3(2H)-one, 4-bromoisoquinoline-1,3(2H,4H)-dione and two α-bromo(phenyl)acetamides were examined under various conditions (base, solvent, thiophile, tempera
Externí odkaz:
https://doaj.org/article/cec7352d017942fd92b34b3870f3c1d6
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 527-539 (2021)
A highly modular method for the synthesis of (Z)-3-[amino(phenyl/methyl)methylidene]-1,3-dihydro-2H-indol-2-ones starting from easily available 3-bromooxindoles or (2-oxoindolin-3-yl)triflate and thioacetamides or thiobenzamides is described. A serie
Externí odkaz:
https://doaj.org/article/c1114a7d759a469d8c21af1d794b004b
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1317-1348 (2018)
This review covers all known examples of [3 + 2]-cycloaddition between sydnones and both terminal as well as internal alkynes/cycloalkynes taken from literature since its discovery by Huisgen in 1962 up to the current date. Except enumeration of synt
Externí odkaz:
https://doaj.org/article/8baef8334f004bb88b0f876cbf83cada
Publikováno v:
Crystals, Vol 2, Iss 2, Pp 349-361 (2012)
Three N-substituted 5-chlorosalicylamides (4-chlorophenyl, 2a; benzyl, 2b; phenethyl 2c) differing in the length of the 'linker' between the benzene ring and the amide moiety were prepared in order to compare their supramolecular architecture. The in
Externí odkaz:
https://doaj.org/article/dd6f60f5eede4585a4d5eff13d84f412
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o413-o413 (2009)
The title molecule, C13H17ClN3OS+·Br−, consists of benzene and pyrrolidine rings and an S–C(NHCH3)2 group. The central C—N bond lengths in the S–C(NHCH3)2 fragment indicate partial double-bond character. Molecules are interconnected into cha
Externí odkaz:
https://doaj.org/article/21c85eab0eb44d8e885b16ab9b192f7b
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o411-o412 (2009)
In the title molecular salt, C11H13ClN3OS+·Br−, the C—N bond lengths in the –S–C(NH2)2 fragment indicate partial double-bond character of these bonds. The constituent ions are connected by N—H...Br bridges into Z-shaped chains. The supramo
Externí odkaz:
https://doaj.org/article/2acf15c4545e4f0b9741cd58491cc766
Autor:
Joseph M. Mwansa, Matthew J. Stirling, Gemma Sweeney, Jiří Hanusek, Jiří Váňa, Michael I. Page
Publikováno v:
Dalton Transactions. 51:2696-2707
The novel dimeric iodo-iridium(iii) complex bearing an amide moiety within the tetramethylcyclopentadiene ring, has been synthesised, characterised and its catalytic activity has been evaluated in the transfer hydrogenation of imines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1ac2620b96dfa90b0b9f98e5f2f25f5
https://doi.org/10.1039/d2dt00149g
https://doi.org/10.1039/d2dt00149g
Publikováno v:
The Journal of organic chemistry. 86(15)
A novel synthetic approach involving an Eschenmoser coupling reaction of substituted 3-bromooxindoles (H, 6-Cl, 6-COOMe, 5-NO2) with two substituted thiobenzanilides in dimethylformamide or acetonitrile was used for the synthesis of eight kinase inhi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce290c7b2fa1ed58b08e9fc20d94ece3
https://pubmed.ncbi.nlm.nih.gov/34269051
https://pubmed.ncbi.nlm.nih.gov/34269051
Autor:
Kamila Dostálová, Eva Horáková, Pavel Drabina, Jiří Váňa, Jakub Valtr, Jiří Hanusek, Aleš Růžička
Publikováno v:
ChemistrySelect. 4:3973-3979
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66fda3d5875010cb5d70966e63ffe72e
https://doi.org/10.1002/slct.201900481
https://doi.org/10.1002/slct.201900481