Recent years have witnessed a heightened interest in the chemistry of depaipeptidea. Unfortunately, the methods uaed at present for investigating this class of compounda are quite restricted and not very specific. We therefore considered it
Mass spectrometric study of cyclodepsipeptides. Staphylomycin S
β Scribed by A.A. Kiryushkin; V.M. Burikov; B.V. Rosinov
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 240 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
PRBVIOUSLY we have shown (l-5) that the mass spectrometric method can be successfully used for rapid determination of cyclic di-, tetra-end hexsdepeipeptide structures with various sequences of amino and hydroxy acid residues.
π SIMILAR VOLUMES
## Ol m2 q l -m 2
A mass spectrometric study of several para-substituted benzylidenecyanoacetamides was performed; thus, electron impact, chemical ionization and fast atom bombardment mass spectrometric studies for each molecule were acquired and then compared in order to establish a general fragmentation pattern. In
be stored at low temperature (--40 " C ) if decomposition is to be avoided. As expected, the new sulfur modification is only slightly vaporizable without decomposition even under high vacuum, as is shown by the mass spectrum [81.