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Org Lett ; 21(20): 8449-8453, 2019 10 18.
Article in English | MEDLINE | ID: mdl-31591889

ABSTRACT

The bioactivity-guided examination of a Leptolyngbya sp. led to the isolation of leptazolines A-D (1-4), from the culture media, along with two degradation products (5 and 6). Density functional theory nuclear magnetic resonance calculations established the relative configurations of 1 and 2 and revealed that the calculated shifts depended on the operating system when using the "Willoughby-Hoye" Python scripts to streamline the processing of the output files, a previously unrecognized flaw that could lead to incorrect conclusions.


Subject(s)
Cyanobacteria/chemistry , Oxazoles/chemical synthesis , Magnetic Resonance Spectroscopy/standards , Molecular Structure , Oxazoles/chemistry , Reference Standards , Stereoisomerism
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