N.m.r. studies of the conformation of analogues of methyl β-lactoside in methyl sulfoxide-d6
✍ Scribed by Alfonso Rivera-Sagredo; Jesús Jiménez-Barbero; Manuel Martín-Lomas
- Book ID
- 107726038
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 633 KB
- Volume
- 221
- Category
- Article
- ISSN
- 0008-6215
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The conformation in solution in methyl sulfoxide of the immunoadjuvant peptidoglycan monomer (PGM), obtained by digestion with lysozyme of the linear peptidoglycan polymer isolated from Brevibacaerium divaticatum, was studied by 'H-n.m.r. spectroscopy. The temperature dependence of the chemical shif
## Abstract Thiosemicarbazones are having the ability to bind with metal and inhibit the enzyme ribonucleoside diphosphate reductase (RDR), an enzyme which is involved in the synthesis of DNA precursors in the mammalian cells. The title compound N‐methyl‐t‐3‐methyl‐r‐2, c‐6‐diphenylpiperidin‐4‐one