Abstract
This paper describes the construction of three key intermediates
for a projected total synthesis of the marine alkaloid
zoanthamine. These building blocks, corresponding to the C1-C5,
C6-C10 and C11-C24 fragments of the target molecule, are
synthesised efficiently form (R)-hydroxymethyl-butyrolactone,
methyl propiolate, and (S)-prillyl alcohol, respectively.
Original language | English |
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Journal | Acta Chem. Scand. |
Volume | 51 |
Pages (from-to) | 1217-1223 |
Publication status | Published - 1997 |