Chris Welch
Reductive Amination-A convenient method for generating diverse, mono-functionalised 5,10,15,20-tetraphenyl porphyrins
Welch, Chris; Archibald, Stephen; Welch, Christopher; Archibald, Stephen J.; Boyle, Ross
Authors
Stephen Archibald
Christopher Welch
Professor Steve Archibald S.J.Archibald@hull.ac.uk
Professor in Molecular Imaging
Professor Ross Boyle R.W.Boyle@hull.ac.uk
Professor of Biological Chemistry
Abstract
Formylation followed by reductive amination of 5,10,15,20-tetraphenyl porphyrin (TPP) is shown to be a versatile synthetic procedure for monosubstitution of the porphyrin core re-giospecifically at one β-position. A diverse range of substituents can be introduced in this way in good yields, including cyclen aza-crown macrocycles. © Georg Thieme Verlag Stuttgart.
Citation
Welch, C., Archibald, S. J., & Boyle, R. (2009). Reductive Amination-A convenient method for generating diverse, mono-functionalised 5,10,15,20-tetraphenyl porphyrins. SYNTHESIS, 2009(4), 551-556. https://doi.org/10.1055/s-0028-1083335
Journal Article Type | Article |
---|---|
Online Publication Date | Jan 27, 2009 |
Publication Date | 2009-01 |
Journal | SYNTHESIS-STUTTGART |
Print ISSN | 0039-7881 |
Electronic ISSN | 1437-210X |
Publisher | Thieme Gruppe |
Peer Reviewed | Peer Reviewed |
Volume | 2009 |
Issue | 4 |
Pages | 551-556 |
DOI | https://doi.org/10.1055/s-0028-1083335 |
Keywords | porphyrin, conjugation, macrocycle |
Public URL | https://hull-repository.worktribe.com/output/395920 |
Publisher URL | https://www.thieme-connect.com/ejournals/abstract/10.1055/s-0028-1083335 |
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