Novel Bronchodilators: Synthesis, Transamination Reactions, and Pharmacology of a Series of Pyrazino[2,3- c ][1,2,6]thiadiazine 2,2-Dioxides
✍ Scribed by Campillo, Nuria; García, Concepción; Goya, Pilar; Alkorta, Ibon; Páez, Juan A.
- Book ID
- 120934362
- Publisher
- American Chemical Society
- Year
- 2000
- Tongue
- English
- Weight
- 169 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-2623
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## Abstract The synthesis of novel analogues of foric acid (FA) antagonists derived from the pyrazino[2,3‐c]‐1,2,6‐thiadiazine 2,2‐dioxide system incorporating the glutamic acid side chain at the 7‐position is described. No significant DHFR inhibition of cytotoxic activity has been found with these
One pot alkoxylation at position 7 of 6-arylpyrazino [2,3c][1,2,6]thiadiazine 2,2-dioxides with NBS or NCS in the appropriate alcohol is described. Rationalization of the mechanism of the reaction, which does not proceed through the in-
## GI ucosidationa of Q a m i n o -8 H -p ~o C 3 -c l [1,2,6llrhiadiazifie 2.2dioxide and its 6,7-dimetbyi-and 6,7-diphenyi derivatives via the "siiylation method" are described. The reaction favors N-1 substitution and the te~-U-acetylglucopyranosyl derivatives j, 6, and 7 as well as the free nud