Syntheses and Radical Polymerization Behavior of Methacrylamides Having Peptide Moieties: Effect of the Methylene Chain Introduced between the Methacrylamide and Peptide Moieties on the Polymerizability and Polymer Structure
- 1 May 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 30 (10) , 2902-2906
- https://doi.org/10.1021/ma970131t
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Highly Radical-Polymerizable Methacrylamide Having Dipeptide Structure. Synthesis and Radical Polymerization of N-Methacryloyl-l-leucyl-l-alanine Methyl EsterMacromolecules, 1996
- Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phasesJournal of Chromatography A, 1994
- Synthesis of Optically Active Polymethacrylates Bearing Axially Dissymmetric 1,1′-Binaphthalene Skeleton as a Pendant Group and Their Optical Resolution Ability as Chiral Adsorbent for HPLCBulletin of the Chemical Society of Japan, 1992
- Synthesis and polymerization of .gamma.-trichloroethyl-L-glutamate N-carboxyanhydride: a polypeptide that can be functionalized with a nucleophilic agentJournal of the American Chemical Society, 1988
- Asymmetric epoxidation of electron-poor olefins-VTetrahedron, 1984
- The circular dichroism of the β structure of poly-l-lysineBiochemical and Biophysical Research Communications, 1966