Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kadir Aksu"'
Autor:
Kadir Aksu, Mehmet Kaya
Publikováno v:
ACS Omega, Vol 9, Iss 3, Pp 3701-3708 (2024)
Externí odkaz:
https://doaj.org/article/9dbf18ccce2c4a0cba35eabd35b47967
Autor:
Kadir Aksu
Publikováno v:
Volume: 11, Issue: 3 2152-2159
Journal of the Institute of Science and Technology
Journal of the Institute of Science and Technology
Benzoic acid, methyl benzoate compounds and their derivatives are valuable compounds that have a wide range of activities and synthesis of these is important for organic chemists. In this study, the synthesis of methyl-4,5-dimethoxy-2-(2-(4-methoxyph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b41195bc6b1ad8f3eca71d8a4cdc513
https://doi.org/10.21597/jist.875097
https://doi.org/10.21597/jist.875097
Publikováno v:
Organic Communications, Vol 12, Pp 38-42 (2019)
In this work, new N-substituted 2-aminopyrrole derivatives were synthesized. Initially, some crotonitriles were prepared by condensation of malononitrile with arylmethylketones, which was followed by conversion of them to the bromocrotonitriles. Fina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4981e9c56d04abcf88009720fdb51c90
https://www.acgpubs.org/doc/201903311405224-55-OC-1903-1222.pdf
https://www.acgpubs.org/doc/201903311405224-55-OC-1903-1222.pdf
Publikováno v:
Chemistrybiodiversity. 18(10)
In this work, the inhibitory effect of some symmetric sulfamides derived from phenethylamines were determined against human carbonic anhydrase (hCA) I, and II isoenzymes, and compared with standard compound acetazolamide. IC50 values were obtained fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7439741d16c199a100ae1b692fd5c471
https://pubmed.ncbi.nlm.nih.gov/34387019
https://pubmed.ncbi.nlm.nih.gov/34387019
Publikováno v:
Archiv der PharmazieREFERENCES. 354(2)
The regio- and stereospecific synthesis of O-methyl-chiro-inositols and O-methyl-scyllo-inositol was achieved, starting from p-benzoquinone. After preparing dimethoxy conduritol-B as a key compound, regiospecific bromination of the alkene moiety of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87e167951c212da4110858769824d0b0
https://pubmed.ncbi.nlm.nih.gov/32997390
https://pubmed.ncbi.nlm.nih.gov/32997390
Publikováno v:
Tetrahedron Letters. 59:1258-1260
The regio- and stereospecific synthesis of dl -4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol is reported. Bromination of p-benzoquinone followed by reduction of the carbonyl groups with NaBH4 gave the corresponding trans-dibromodiol compound, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07071a30f0d22a1a9e36a5eecf695d7c
https://doi.org/10.1016/j.tetlet.2018.02.050
https://doi.org/10.1016/j.tetlet.2018.02.050
Publikováno v:
Archiv der Pharmazie. 349:944-954
A series of ureas derived from phenethylamines were synthesized and evaluated for human carbonic anhydrase (hCA) I and II, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE) enzyme inhibitory activities and antioxidant properties. The urea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8193b13d3613a14e16b49cbfd8f2b067
https://doi.org/10.1002/ardp.201600183
https://doi.org/10.1002/ardp.201600183
Publikováno v:
Archiv der Pharmazie. 354:2000254
The regio- and stereospecific synthesis of O-methyl-chiro-inositols and O-methyl-scyllo-inositol was achieved, starting from p-benzoquinone. After preparing dimethoxy conduritol-B as a key compound, regiospecific bromination of the alkene moiety of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da07e4ea8547a047688063221564300e
https://doi.org/10.1002/ardp.202000254
https://doi.org/10.1002/ardp.202000254
Publikováno v:
Archiv der Pharmazie. 348:446-455
The antioxidant and acetylcholinesterase inhibitory properties of novel symmetric sulfamides derived from phenethylamines were evaluated. Phenethylamines 8-11 were reacted with SO2Cl2 in the presence of Et3N to afford sulfamides in good yields. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::862d3ffd20f382e4748d70df7fdae163
https://doi.org/10.1002/ardp.201500035
https://doi.org/10.1002/ardp.201500035
Publikováno v:
Synthetic Communications. 45:78-85
Dopamine, rotigotin, ladostigil, and rasagiline analogues 2-amino-4,5,6-trimethoxyindane and 1-amino-5,6,7-trimethoxyindane were synthesized starting from 5,6,7-trimethoxyindan-1-one for the first time with 34% and 45% total yields. α-Carboxylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d39f81fa3028ea1ba7a05d3d331b19
https://doi.org/10.1080/00397911.2014.957321
https://doi.org/10.1080/00397911.2014.957321