Synthesis and biological activity of enantiomers of a conformationally restricted muscarone analog
โ Scribed by Edwin S.C. Wu; Robert A. Mack; Alex Kover; James T. Loch III; George Mullen; Robert J. Murray; John C. Gordon; Anthony C. Machulskis; Sally A. McCreedy; James C. Blosser
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 321 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Abslrart: The synthesis of a new, conformationally restrained a~log of tryptoghan, 1,2,3,4ktrahydtv-2-ami-2-mrboxy\_cyflopentfbJindole (5) is descrhd. The key step involzm the BF3-Et,0 catalyzed intramolecular cycl&atian of adinoketone 2b into the lt3,4tetrahydro\_~~ (3). Conformationally restricted
The synthesis of 5-hydroxy-l-[[(5-nitro-2-furanyl)methylenelamino] -2,4-imidazolidinedione is described, and its antibacterial activity is reported. Keyphrases Nitrofurantoin analog-synthesized, screened for antibacterial activity 2,4-Imidazolidinedione, substituted-synthesized, screened for antiba