Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides.
Publication
, Journal Article
Becker, ML; Liu, J; Wooley, KL
Published in: Chemical communications (Cambridge, England)
January 2003
A novel strategy for the preparation of peptidic-synthetic bioconjugate block copolymers is based upon sequential condensation and living radical addition polymerizations, each performed upon a solid support.
Duke Scholars
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Published In
Chemical communications (Cambridge, England)
DOI
EISSN
1364-548X
ISSN
1359-7345
Publication Date
January 2003
Issue
2
Start / End Page
180 / 181
Related Subject Headings
- Resins, Synthetic
- Protein Structure, Secondary
- Polymers
- Peptides
- Organic Chemistry
- Nitrogen Oxides
- Combinatorial Chemistry Techniques
- Amino Acid Sequence
- 40 Engineering
- 34 Chemical sciences
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Becker, M. L., Liu, J., & Wooley, K. L. (2003). Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides. Chemical Communications (Cambridge, England), (2), 180–181. https://doi.org/10.1039/b209557b
Becker, Matthew L., Jianquan Liu, and Karen L. Wooley. “Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides.” Chemical Communications (Cambridge, England), no. 2 (January 2003): 180–81. https://doi.org/10.1039/b209557b.
Becker ML, Liu J, Wooley KL. Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides. Chemical communications (Cambridge, England). 2003 Jan;(2):180–1.
Becker, Matthew L., et al. “Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides.” Chemical Communications (Cambridge, England), no. 2, Jan. 2003, pp. 180–81. Epmc, doi:10.1039/b209557b.
Becker ML, Liu J, Wooley KL. Peptide-polymer bioconjugates: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides. Chemical communications (Cambridge, England). 2003 Jan;(2):180–181.
Published In
Chemical communications (Cambridge, England)
DOI
EISSN
1364-548X
ISSN
1359-7345
Publication Date
January 2003
Issue
2
Start / End Page
180 / 181
Related Subject Headings
- Resins, Synthetic
- Protein Structure, Secondary
- Polymers
- Peptides
- Organic Chemistry
- Nitrogen Oxides
- Combinatorial Chemistry Techniques
- Amino Acid Sequence
- 40 Engineering
- 34 Chemical sciences