Sub-structure syntheses and relative stereochemistry in the bistramide (bistratene) series of marine metabolites

Author(s)
Gallagher, PO
McErlean, CSP
Jacobs, MF
Watters, DJ
Kitching, W
Griffith University Author(s)
Year published
2002
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Abstract
The (6R*,9S*,11S*) and (22S*,23R*,27R*,31R*) stereochemistry, respectively, of the tetrahydropyranyl and spiroacetal moieties in bistramide A (1) have been established by stereoselective syntheses and high field NMR comparisons. Routes to the ?-amino acid moiety are outlined.
Journal Title
Tetrahedron Letters
Volume
43
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Copyright Statement
© 2002 Elsevier : Reproduced in accordance with the copyright policy of the publisher : This journal is available online - use hypertext links.
Subject
Medicinal and biomolecular chemistry
Organic chemistry
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