Issue 24, 2002

First total synthesis of the marine illudalane sesquiterpenoid alcyopterosin E

Abstract

The first synthesis of the marine illudalane sesquiterpenoid alcyopterosin E was accomplished through a concise ABC ring-formation strategy using a rhodium(I)-catalysed intramolecular alkyne cyclotrimerisation as key connection.

Graphical abstract: First total synthesis of the marine illudalane sesquiterpenoid alcyopterosin E

Supplementary files

Article information

Article type
Communication
Submitted
01 Oct 2002
Accepted
24 Oct 2002
First published
08 Nov 2002

Chem. Commun., 2002, 2984-2985

First total synthesis of the marine illudalane sesquiterpenoid alcyopterosin E

B. Witulski, A. Zimmermann and N. D. Gowans, Chem. Commun., 2002, 2984 DOI: 10.1039/B209573D

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