Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Panayiotis Koutentis"'
Autor:
Panayiotis Koutentis
Publikováno v:
ARKIVOC, Vol 2017, Iss 3, Pp 1-8 (2016)
Externí odkaz:
https://doaj.org/article/ff10e3e9f6254d8aa098116c1e8a2f59
Publikováno v:
Molbank. 2023:M1560
Reaction of methyl 3-bromo-5-cyanoisothiazole-4-carboxylate with conc. H2SO4 gave methyl 3-bromo-5-carbamoylisothiazole-4-carboxylate in 93% yield. The compound was fully characterized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::784e8779397eff3d26df6d39db891b97
https://doi.org/10.3390/m1560
https://doi.org/10.3390/m1560
Publikováno v:
Molbank. 2023:M1553
A reaction of 3-chloroisothiazole-5-carbonitrile with 1-iodo-4-methylbenzene (2 equiv.) produced 3-chloro-4-(p-tolyl)isothiazole-5-carbonitrile in a 60% yield. The compound was fully characterized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4651bceb923860ee9056d72f4128da57
https://doi.org/10.3390/m1553
https://doi.org/10.3390/m1553
Publikováno v:
Molbank. 2022:M1354
Reaction of 4,5-dichloro-1,2,3-dithiazolium chloride with 2-[amino(methylthio)methylene])malononitrile (1 equiv) in the presence of pyridine (2 equiv) gave (Z)-2-{[(4-chloro-5H-1,2,3-dithiazol-5-ylidene)amino](methylthio)methylene}malononitrile in 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1843491badce9bdd522804905be52ed6
https://doi.org/10.3390/m1354
https://doi.org/10.3390/m1354
Publikováno v:
Molbank. 2022:M1321
3,5-Dichloro-4H-1,2,6-thiadiazin-4-one reacts with benzo[d]thiazole-2-thiol (1 equiv) and triethylamine (1 equiv) to give 3-(benzo[d]thiazol-2-ylthio)-5-chloro-4H-1,2,6-thiadiazin-4-one in 71% yield. The reactivity of this compound with methoxide is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6b5aed1ad91fcf985443ecd5d5da027
https://doi.org/10.3390/m1321
https://doi.org/10.3390/m1321
Autor:
Panayiotis Koutentis
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 10, Iss 2, Pp 346-359 (2005)
Scopus-Elsevier
Molecules; Volume 10; Issue 2; Pages: 346-359
Molecules, Vol 10, Iss 2, Pp 346-359 (2005)
Scopus-Elsevier
Molecules; Volume 10; Issue 2; Pages: 346-359
A series of monosubstituted acetonitriles were treated with disulfur dichloride at room temperature in CH 2 Cl 2 to afford 5-substituted-4-chloro-1,2,3-dithiazolium chlorides 1 . Where the 5-substituent was not a good leaving group the chloride salts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985710d9aa0f4688c9aee2179936f15a
https://pubmed.ncbi.nlm.nih.gov/18007305
https://pubmed.ncbi.nlm.nih.gov/18007305
Autor:
ILYAS YILDIRIM, Martin Paterson, Rajkumar Banerjee, Styliana Mirallai, Neerasa Jayaprakash, Christos Constantinides, Atsuo Nakazaki, Panayiotis Koutentis, Levy Cao, Zachary Houston, Henry N. C. Wong
Publikováno v:
Organic & Biomolecular Chemistry. 12:6527
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d8b9647c5e4e98978e5cdf3c853a1f9
https://doi.org/10.1039/c4ob90098g
https://doi.org/10.1039/c4ob90098g
Autor:
Georgia Melagraki, Haralambos Sarimveis, Panayiotis Koutentis, John Markopoulos, Olga Igglessi-Markopoulou
Publikováno v:
Journal of Molecular Modeling; Jan2007, Vol. 13 Issue 1, p55-64, 10p