Synthesis and Antimicrobial Activity of 4 H -4-Oxoquinolizine Derivatives: Consequences of Structural Modification at the C-8 Position
โ Scribed by Ma, Zhenkun; Chu, Daniel T. W.; Cooper, Curt S.; Li, Qun; Fung, Anthony K. L.; Wang, Sanyi; Shen, Linus L.; Flamm, Robert K.; Nilius, Angela M.; Alder, Jeffery D.; Meulbroek, Jonathan A.; Or, Yat Sun
- Book ID
- 120057905
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 221 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-2623
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AbstractรAmong the hapalosin derivatives synthesized, the compounds carrying methyl (5a), methylthioethyl (5d) and phenylmethyl (5e) groups at the C12 position possess only the cis-peptide structure, in contrast to the cases of 5b and 5c. In addition to their conformational stability, the biological
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