Journal article
Synthesis of mono and Bis[60]fullerene-based dicationic peptoids
European Journal of Organic Chemistry, Vol.2015(1), pp.195-201
2015
Abstract
Increasing numbers of biological applications of fullerenyl amino acids and their derivatives encouraged us to synthesise [60]fullerenyldihydropyrrole peptides, prepared from the coupling of mono- and bis[60]fullerenyldihydropyrrolecarboxylic acids 4, 5 and 41 with presynthesised peptides 13, 16, 24, 28, 29 and 46. The resulting hydrophobic scaffolded di- and tetra-cationic derivatives were tested against Staphylococcus aureus NCTC 6571 and Escherichia coli NCTC 10418. The synthesis, characterisation and biological results are discussed in this paper.
Details
- Title
- Synthesis of mono and Bis[60]fullerene-based dicationic peptoids
- Authors/Creators
- S. Jennepalli (Author/Creator)K.A. Hammer (Author/Creator)T.V. Riley (Author/Creator)S.G. Pyne (Author/Creator)P.A. Keller (Author/Creator)
- Publication Details
- European Journal of Organic Chemistry, Vol.2015(1), pp.195-201
- Publisher
- Wiley-VCH Verlag
- Identifiers
- 991005543321107891
- Copyright
- © 2014 SIOC, CAS, Shanghai, & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites
Metrics
140 File views/ downloads
40 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- Citation topics
- 2 Chemistry
- 2.76 2D Materials
- 2.76.532 Fullerene Chemistry
- Web Of Science research areas
- Chemistry, Organic
- ESI research areas
- Chemistry