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Wipf et al., 1993 - Google Patents

Total synthesis and structure assignment of the antitumor antibiotic aranorosin

Wipf et al., 1993

Document ID
715001152503349042
Author
Wipf P
Kim Y
Fritch P
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

The structurally unique antifungal and antitumor antibiotic aranorosin was prepared in a convergent, stereoselective sequence. Oxidative cyclization of AT-protected L-tyrosine, followed by face-selective 1, 2-addition of [(benzyloxy) methyl] lithium, Henbest oxidation in …
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    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
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    • C07F7/1848C1 being an unsubstituted acyclic saturated hydrocarbon radical containing less than six carbon atoms, a benzyl radical, a phenyl radical, or a methyl substituted phenyl radical
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    • C07D213/06Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom

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