Results 91 to 100 of about 331 (145)
Some of the next articles are maybe not open access.
Synthesen bicyclischer 1,2,6‐Thiadiazine
Archiv der Pharmazie, 1981Abstractα‐Aminosäureamide aus der Pyrrol‐ Furan‐ und Thiophen‐Reihe werden zu neuen Schwefelheterocyclen umgesetzt. Die Stabilität dieser Verbindungen wird untersucht.
Wolfgang Offermann +2 more
openaire +1 more source
Organic Letters, 2015
Condensation of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine with a range of anilines gave 22 N-aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines in 43-96% yields. The scope and limitations of this condensation are briefly investigated. Furthermore, mono- and bis-substitution of the C-3 and C-5 chlorines of 3,5-dichloro-N-phenyl-4H-1,2,6-thiadiazin-4-imine by
Kalogirou, Andreas S. +5 more
openaire +4 more sources
Condensation of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine with a range of anilines gave 22 N-aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines in 43-96% yields. The scope and limitations of this condensation are briefly investigated. Furthermore, mono- and bis-substitution of the C-3 and C-5 chlorines of 3,5-dichloro-N-phenyl-4H-1,2,6-thiadiazin-4-imine by
Kalogirou, Andreas S. +5 more
openaire +4 more sources
Chemischer Informationsdienst, 1985
AbstractDie durch Ringschluß hergestellten Thiadiazin‐dioxide (II) und (IV) zeigen keine herbizide Wirksamkeit.
P. GOYA +3 more
openaire +1 more source
AbstractDie durch Ringschluß hergestellten Thiadiazin‐dioxide (II) und (IV) zeigen keine herbizide Wirksamkeit.
P. GOYA +3 more
openaire +1 more source
Cyclisation chemistry of 4H-1,2,6-thiadiazines
Journal of the Chemical Society, Perkin Transactions 1, 20003,5-Dichloro-4H-1,2,6-thiadiazin-4-one 1 condenses rapidly at room temperature with 1,2-diaminobenzene, 2-aminothiophenol and sodium 2-aminophenoxide to give, respectively, the purple thiadiazinoquinoxaline 4a, red thiadiazinobenzothiazine 4b and orange thiadiazinobenzoxazine 4c in almost quantitative yield.
Koutentis, Panayiotis Andreas +3 more
openaire +2 more sources
Chemistry of 4-dicyanomethylene-1,2,6-thiadiazines
Journal of the Chemical Society, Perkin Transactions 1, 2000The chlorine atoms in 3,5-dichloro-4-dicyanomethylene-1,2,6-thiadiazine 1 are readily displaced by thiophenols in the presence of Hunig’s base, the first at −78 °C and the second at 20 °C to give the orange mono- and bis-arylthio derivatives in high yield (Table 1).
Koutentis, Panayiotis Andreas +3 more
openaire +2 more sources
Structure of 1,2,6‐thiadiazine 1,1‐dioxides
Journal of Physical Organic Chemistry, 1990AbstractAb initio theoretical calculations were carried out on the three tautomers, NH, OH and CH, of 1,2,6‐thiadiazine 1,1‐dioxides. Different basis sets were employed in order to obtain an adequate description of these cyclic sulphamide derivatives.
José Elguero +6 more
openaire +1 more source
Fused 1,2,6‐Thiadiazines Tetrahydrobenzo[b]thieno[2,3‐c] [1,2,6]thiadiazine 2,2‐Dioxides
Archiv der Pharmazie, 1984AbstractSuitably substituted derivatives of tetrahydrobenzo[b]thiophene were treated with sulfamoyl chlorides to give sulfamoyl esters and nitriles. Ring closure of these compounds, under various conditions, afforded tetrahydrobenzo[b]thieno[2,3‐c][1,2,6]thiadiazine 2,2‐dioxides. Their herbicidal activities were tested.
Pilar Goya +3 more
openaire +1 more source
ChemInform, 2010
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Andreas S. Kalogirou +2 more
openaire +2 more sources
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Andreas S. Kalogirou +2 more
openaire +2 more sources
Tetrahedron, 2010
Abstract [3,5-Bis(dialkylamino)-4H-1,2,6-thiadiazin-4-ylidene]propanedinitriles 6a–c, react with sodium methoxide or ethoxide to give the corresponding 6-alkoxy-4-dialkylamino substituted pyrrolo[2,3-c][1,2,6]thiadiazine-5-carbonitriles 7a–f in variable yields.
Kalogirou, Andreas S. +5 more
openaire +2 more sources
Abstract [3,5-Bis(dialkylamino)-4H-1,2,6-thiadiazin-4-ylidene]propanedinitriles 6a–c, react with sodium methoxide or ethoxide to give the corresponding 6-alkoxy-4-dialkylamino substituted pyrrolo[2,3-c][1,2,6]thiadiazine-5-carbonitriles 7a–f in variable yields.
Kalogirou, Andreas S. +5 more
openaire +2 more sources

