01037nas a2200229 4500008004100000022001400041245005600055210005500111260007500166300001200241520026000253653002000513653001400533653003300547653002800580653002000608100002800628700002100656700002600677700002300703856008100726 2007 eng d a0936-521400aSynthesis of the C19-C34 segment of amphidinolide C0 aSynthesis of the C19C34 segment of amphidinolide C aRUDIGERSTR 14, D-70469 STUTTGART, GERMANYbGEORG THIEME VERLAG KGcMAR a567-5703 a

The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski's Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.

10aamphidinolide C10aCytotoxic10aNozaki-Hiyama-Kishi coupling10aRing-closing metathesis10aWittig reaction1 aMohapatra, Debendra, K.1 aRahaman, Hasibur1 aChorghade, Mukund, S.1 aGurjar, Mukund, K. uhttps://library.ncl.res.in/content/synthesis-c19-c34-segment-amphidinolide-c