Zobrazeno 1 - 10
of 57
pro vyhledávání: '"E. P. PAPADOPOULOS"'
Publikováno v:
Frontiers in Drug Discovery, Vol 4 (2024)
Reversible phosphorylation is the basis for signal transduction in eukaryotic cells, and this is tightly controlled by the complex interplay of kinases and phosphatases. Many malignancies are characterized by dysregulation of the delicate protein pho
Externí odkaz:
https://doaj.org/article/01d3318abf6e40219aedb51d5194df09
Publikováno v:
Journal of Heterocyclic Chemistry. 40:885-893
The triethylamine-catalyzed reactions of methyl N-(cyanothioformyl)anthranilate (1) with isocyanates result in cyclization involving the cyano group to form methyl 2-(4-imino-2-oxo-3-substituted-5-thioxoimi-dazolidin-1-yl)benzoates (4). Ring closure
Publikováno v:
Journal of Heterocyclic Chemistry. 38:343-347
A variety of 2-substituted thiophenes is readily obtained from 2-(2-thienyl)-4H-3,l-benzothiazin-4-one (2), which is formed when thiophene reacts with methyl 2-isothiocyanatobenzoate (1) in the presence of anhydrous stannic chloride.
Autor:
L. M. Deck, E. P. Papadopoulos
Publikováno v:
Journal of Heterocyclic Chemistry. 37:675-680
The ureas 3 which are obtained from 3-(benzylamino)propanenitrile (1) and various isocyanates (2) cyclize readily upon heating in ethanol, in the presence of hydrochloric acid, to form 3-substituted 1-benzyldihydro-2,4-(1H,3H)pyrimidinediones (11) in
Publikováno v:
ChemInform. 32
A variety of 2-substituted thiophenes is readily obtained from 2-(2-thienyl)-4H-3,l-benzothiazin-4-one (2), which is formed when thiophene reacts with methyl 2-isothiocyanatobenzoate (1) in the presence of anhydrous stannic chloride.
Publikováno v:
ChemInform. 35
The triethylamine-catalyzed reactions of methyl N-(cyanothioformyl)anthranilate (1) with isocyanates result in cyclization involving the cyano group to form methyl 2-(4-imino-2-oxo-3-substituted-5-thioxoimi-dazolidin-1-yl)benzoates (4). Ring closure
Autor:
E. P. Papadopoulos, L. M. Deck
Publikováno v:
ChemInform. 32
The ureas 3 which are obtained from 3-(benzylamino)propanenitrile (1) and various isocyanates (2) cyclize readily upon heating in ethanol, in the presence of hydrochloric acid, to form 3-substituted 1-benzyldihydro-2,4-(1H,3H)pyrimidinediones (11) in
Autor:
E. P. Papadopoulos, L. L. Whitfield
Publikováno v:
Synthesis. 1985:423-426
Le compose du titre reagit avec des amines ou des alcanols-1: obtention des dialkylthiocarbamoylamides ou alcoxythiocarbonylamides et esters de methyle de l'acide phtalique; l'action de l'hydrazine sur les alcoxythiocarbonylamides conduit aux s-triaz
Autor:
E. P. Papadopoulos
Publikováno v:
The Journal of Organic Chemistry. 41:962-965
Autor:
E. P. Papadopoulos
Publikováno v:
Journal of Heterocyclic Chemistry. 21:1411-1414
The urea 1 obtained from anthranilonitrile and 3-chloropropyl isocyanate is converted into 3-(3-chloropropyl)-2,4(1H,3H)quinazolinedione (4) when heated with hydrochloric acid, whereas it undergoes a double cyclization to form 2,3,4,7-tetrahydro-6H-p