1977
DOI: 10.1002/zfch.19770170104
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Zur Reaktivität von 2‐Hydrazino‐1,3,4‐thiadiazinen

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Cited by 9 publications
(9 citation statements)
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“…The free base was obtained from the filtrate by addition of a conc. solution of NH 3 . The crude product contains 2.…”
Section: -Methylamino-56-diphenyl-6h-134-thiadiazine (1)mentioning
confidence: 99%
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“…The free base was obtained from the filtrate by addition of a conc. solution of NH 3 . The crude product contains 2.…”
Section: -Methylamino-56-diphenyl-6h-134-thiadiazine (1)mentioning
confidence: 99%
“…Method B: A mixture of 4-nitrobenzaldehyde-4-methylthiosemicarbazone (2.38 g, 10 mmol) and 2-bromo-1,2-diphenylethan-1-one (2.75 g, 10 mmol) in EtOH (100 mL) was refluxed for 2 h. After cooling, the mixture was neutralized with NH 3 …”
Section: -Nitrobenzaldehyde-[(3-methyl-45-diphenyl-13-thiazolon-(2mentioning
confidence: 99%
“…1,2,[ 2H-1,3,4]thiadiazines were prepared by cyclization of 4-amino-5-sulfanyl-l,2,4-triazoles with phenacyl bromides. INTRODUCTION 1,3,Thiadiazines are of considerable biochemical and pharmacological relevance. Several 2-amino-1,3,4-thiadiazine derivatives are important matrix metalloproteinase inhibitors [1,2].…”
mentioning
confidence: 99%
“…Several 2-amino-1,3,4-thiadiazine derivatives are important matrix metalloproteinase inhibitors [1,2]. 2-Alkylimino-1,3,4-thiadiazines and 2-alkyamino-1,3,4-thiadiazines are used as cardiotonic and spasmolytic agents [3][4][5][6][7][8]. 1,3,4-Thiadiazin-2-ones are cardiotonics with calcium sensitizing activity [9][10][11].…”
mentioning
confidence: 99%
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