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Novel High Energy Intermediate Analogues with Triazasterol-related Structures as Inhibitors of the Ergosterol Biosynthesis V [1]. Synthesis of Hexahydro-5H-imidazo[1′, 2′: 1,2]pyrimido-[4,3-a]isoquinolines and 1-Alkyl Analogues Representing New 8,13,15-Triazasteroids

✍ Scribed by Edith Gößnitzer; Asbjörn Punkenhofer

Publisher
Springer Vienna
Year
2003
Tongue
English
Weight
255 KB
Volume
134
Category
Article
ISSN
0026-9247

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📜 SIMILAR VOLUMES

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 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 129 KB 👁 2 views

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