In:
Chirality, Wiley, Vol. 18, No. 6 ( 2006-01), p. 413-418
Abstract:
Two stereoisomers of ascolactone ( A , B ), natural products with two asymmetric carbon atoms, are isolated from the marine‐derived fungus Ascochyta salicorniae . Although these compounds show virtually opposite CD spectra and [α] D , 1 H‐ and 13 C‐NMR data exclude the presence of enantiomers and suggest ascolactone A and B to be epimeric lactones. By comparing the experimental CD spectra with those calculated employing time‐dependent density functional theory (TDDFT), we elucidate the configuration at one of the asymmetric carbon atoms. Chirality, 2006. © 2006 Wiley‐Liss, Inc.
Type of Medium:
Online Resource
ISSN:
0899-0042
,
1520-636X
Language:
English
Publisher:
Wiley
Publication Date:
2006
detail.hit.zdb_id:
2001237-8
SSG:
12
SSG:
15,3
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