The identification of depsipeptides by chemical ionisation mass spectroscopy.

Abstract
The chemical ionization mass spectra of 7 naturally occurring [antibiotic] depsipeptides and some of their permethylated derivatives were measured. The primary ionization process involves an ester group and not an amide or other functionality. It probably occurs randomly when the molecule contains more than 1 ester link. Unlike electron impact mass spectra, those obtained under chemical ionization conditions gave sequence information for all of the depsipeptides examined or their permethylated derivatives. A mechanism for the primary fragmentation is proposed.

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