Tunable BODIPY derivatives amenable to "click" and peptide chemistry

Hansen, A.M., Sewell, A.L., Pedersen, R.H., Long, D.-L. , Gadegaard, N. and Marquez, R. (2013) Tunable BODIPY derivatives amenable to "click" and peptide chemistry. Tetrahedron, 69(39), pp. 8527-8533. (doi:10.1016/j.tet.2013.05.037)

[img]
Preview
Text
81026.pdf - Published Version
Available under License Creative Commons Attribution No Derivatives.

723kB

Abstract

Novel azido- and amino- functionalised fluorescent probes based on the BODIPY framework have been developed. The probes can be easily and cheaply synthesised, exhibit the highly desirable BODIPY fluorescent properties, and are amenable to “click” and peptide chemistry methodologies. These probes provide a stable and readily available tool amenable for the visualisation of both solution and solid supported events.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Hansen, Dr Anna and Marquez, Dr Rudi and Pedersen, Mr Rasmus and Gadegaard, Professor Nikolaj and Long, Dr De Liang
Authors: Hansen, A.M., Sewell, A.L., Pedersen, R.H., Long, D.-L., Gadegaard, N., and Marquez, R.
College/School:College of Science and Engineering > School of Chemistry
College of Science and Engineering > School of Engineering > Biomedical Engineering
Journal Name:Tetrahedron
Publisher:Elsevier
ISSN:0040-4020
Copyright Holders:Copyright © 2013 The Authors
First Published:First published in Tetrahedron 69(39):8527-8533
Publisher Policy:Reproduced under a Creative Commons License

University Staff: Request a correction | Enlighten Editors: Update this record

Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
504321New Chemistry Approaches for the Next Generation of HealthcareRudi MarquezEngineering & Physical Sciences Research Council (EPSRC)EP/H005692/1CHEM - CHEMISTRY