Carbohydrate degradation products from alkaline treatment of biomass
✍ Scribed by Eero Sjöström
- Book ID
- 103983693
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 403 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0961-9534
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The structures of alkaline degradation products of concanamycin A were elucidated by analysis of their 270 MHz PMR spectra. Concanamycins A, B, and C, produced by Streptomyces diastatochromogenes S45, inhibit the proliferation of the mouse splenic lymphocytes stimulated by concanavalin A.
Cephradine yields an unique alkaline degradation product, which has been identified by proton magnetic resonance, IT-NMR, and mass spectrometry as 2-[6-(1,4-cyclohexadine-lyl) -2.5dioxo -3piperazinyl] -5,6-dihydro -5methyl -2H-1,3thiazine-4carboxylic acid, sodium salt. Keyphrases 0 Cephradine-struct