(+)-Thiazinotrienomycin E: Relative and absolute stereochemistry
β Scribed by Amos B Smith III; Joseph Barbosa; Nobuo Hosokawa; Hiroshi Naganawa; Tomio Takeuchi
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 185 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The complete relative and absolute configurations of (+)-thiazinotrienomycin E, a potent new ansatrienin cancer cell growth inhibitory agent, have been determined via degradation and chemical correlation.
π SIMILAR VOLUMES
The complete relative and absolute stereochemistry of furaquinocins A-G, a family of cytotoxic antibiotics, have been assigned via a combination of X-ray crystallography, NMR analysis of the derived Mosher esters, and chemical correlation. Komiyama et al. at the Kitasato Institute recently reported
The complete relative and absolute stereochemistry of the potent antrfungal antrbrotrcs (+)-mycotriemn I and (+)-mycotrienrn II have been established by chemrcal correlation with the antltumor agent (+)-tnenomycin A Recently, Umezawa and coworkers reported the isolatron of several ansamycin antibiot