Od. Hensens et al., STRUCTURE ELUCIDATION OF AUSTRALIFUNGIN, A POTENT INHIBITOR OF SPHINGANINE N-ACYLTRANSFERASE IN SPHINGOLIPID BIOSYNTHESIS FROM SPORORMIELLA-AUSTRALIS, Journal of organic chemistry, 60(6), 1995, pp. 1772-1776
The structure elucidation of the novel, potent sphinganine N-acyltrans
ferase inhibitor, australifungin (1), from Sporormiella australis is d
escribed. Extensive exchange-broadening phenomena predominantly of the
keto-enol type were observed on the NMR time scale which was resolved
by derivatization to triacetate (2) and tetraacetate (3) derivatives.
Residual exchange broadening in the acetates was attributed to hinder
ed rotation about the C3-C11 single bond which was frozen out into two
conformers at low temperature, The application of 2D NMR techniques t
o the structure elucidation of the acetate derivatives at ambient and
low temperature therefore contributed considerably to the overall stru
cture determination of 1. The conformation and complete relative stere
ochemistry followed from a consideration of the Karplus relationship f
or H-1-H-1 vicinal coupling constants and phase-sensitive NOE data. Te
mperature-dependent NMR experiments suggest an averaged conformational
mixture of four to five forms in solution at ambient temperature wher
eas a predominant conformer 1 is indicated at low temperature with the
enolized beta-keto aldehyde stabilized through internal H-bonding in
the cis-orientation. The triacetate 2 and tetraacetate 3, by contrast,
are enolized in the sterically favored trans configuration. The beta-
keto alcohol derivative australifunginol (6) is also present.