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Novel High Energy Intermediate Analogues with a Triazasterol Structure as Potential Ergosterol Biosynthesis Inhibitors. Part 4. Antimicrobial Activity of Mono-, Bi-, and Tricyclic 8,13,15-Triazasteroid Analogues Including the Synthesis of Novel 4-Alkylamino- and 4-Alkenylamino-9-hydroxypyrimidoisoquinolines.

✍ Scribed by Edith Goessnitzer; Asbjoern Punkenhofer; Neil S. Ryder

Publisher
John Wiley and Sons
Year
2003
Weight
88 KB
Volume
34
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES

Novel High Energy Intermediate Analogues
Novel High Energy Intermediate Analogues with a Triazasterol Structure as Potential Ergosterol Biosynthesis Inhibitors IV: Antimicrobial Activity of Mono-, Bi-, and Tricyclic 8, 13, 15-Triazasteroid Analogues Including the Synthesis of Novel 4-Alkylamino- and 4-Alkenylamino-9-hydroxypyrimidoisoquinolines
✍ Edith Gâßnitzer; AsbjΓΆrn Punkenhofer; Neil S. Ryder πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 200 KB πŸ‘ 2 views
Novel High Energy Intermediate Analogues
Novel High Energy Intermediate Analogues with Triazasterol-Related Structures as Potential Inhibitors of the Ergosterol Biosynthesis. Part 2. Optimization of the Synthesis of 1,6,7,11b-Tetrahydro-2H-pyrimido[4,3-a] Isoquinolin-4-amines as Parent Compounds of Novel 8,13,15-Triazasteroids.
✍ Edith Goessnitzer; Asbjoern Punkenhofer πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons βš– 129 KB πŸ‘ 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.