Results 241 to 250 of about 13,716 (259)

Antiviral 1,3,4-Thiadiazoles

Chemotherapy, 1974
Three antiviral 1,3,4-thiadiazoles caused, when incubated together with 3H-uridine, a reduction of the incorporation rate into acid-insoluble material of FL cells.
Elke Klimke, Marion Tonew
openaire   +2 more sources

Pyridyl‐1,3,4‐thiadiazole; eine neue Variante der Thiadiazol‐Synthese

Helvetica Chimica Acta, 1958
AbstractThiosemicarbazones of aromatic aldehydes react with acetic anhydride to give well‐defined N4,S‐diacetyl derivatives, which readily undergo oxidative cyclisation to 2‐aryl‐4‐acetamido‐1,3,4‐thiadiazoles. From these intermediates, aryl‐thiadiazoles – especially 2‐(2′‐pyridyl)‐1,3,4‐thiadiazole, inaccessible by the common methods – can be obtained
H. Erlenmeyer, P. Hemmerich, Bernhard Prijs   +2 more
openaire   +2 more sources

Hypotensive thiadiazoles

Journal of Medicinal Chemistry, 1972
S. V. Krees, A. M. Grant, A. B. Mauger, W. J. Rzeszotarski, F. W. Wolff   +4 more
openaire   +3 more sources

1,2,4-Thiadiazoles

ChemInform, 1996
David J. Wilkins, Paul A. Bradley
openaire   +2 more sources

Thiadiazoles and selenadiazoles

2007
F. Kurzer, D. H. Reid
openaire   +2 more sources

1,2,4-Thiadiazoles

2022
Jürgen Schatz, Tabea Fritsch, Sebastian Funk   +2 more
openaire   +1 more source

Thiadiazoles

2011
CHIACCHIO, Ugo, Romeo G.
openaire   +1 more source

Chemistry of thiadiazole and thiadiazine S-oxides

Chemical Reviews, 1970
Alexander. Lawson, R. B. Tinkler
openaire   +3 more sources

1,2,3-Thiadiazoles

2022
Vasiliy A. Bakulev, Tetyana V. Beryozkina, Wim Dehaen   +2 more
openaire   +1 more source

1,3,4-Thiadiazoles

2022
Jürgen Schatz, Kemal Gogić, Tobias Benkert   +2 more
openaire   +1 more source