## Abstract Poly(__N__^ε^‐stearyl‐L‐lysine) and poly(__N__^ε^‐pelargonyl‐L‐lysine) were synthesized both by polymerization of __N__^ε^‐pelargonyl and __N__^ε^‐stearyl‐L‐lysine NCA and by acylation of poly(L‐lysine) with pelargonyl and stearyl chloride. This second route has proven to be very useful
The Synthesis and Conformation of High Molecular Weight Poly-ε-carbobenzyloxy-L-lysine and Poly-L-lysine·HCl1,2
✍ Scribed by Fasman, G. D.; Idelson, M.; Blout, E. R.
- Book ID
- 115451921
- Publisher
- American Chemical Society
- Year
- 1961
- Tongue
- English
- Weight
- 515 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The synthesis of poly(ε‐L‐lysine) is described. This is a poly(ε‐amino acid) in which the ε‐amino group of lysine is condensed with the α‐carboxyl group to produce a chain backbone that is a variant of the usual one seen in proteins and the side chain is the α‐amino group. Conformationa
## Abstract __N__‐Carboxy‐(__N__^ϵ^‐benzyloxycarbonyl)‐L‐lysine anhydride (Z‐L‐lysine NCA) was polymerized in dimethylformamide with triethylamine, diethylamine or hexylamine as initiator, at varying molar ratios of NCA to initiator (M/I ratio). After removal of the protecting Z‐group the resulting