Abstract
The reaction of an amine bearing an amidopyridine recognition site and an aldehyde bearing a carboxylic acid recognition site affords an imine that is capable of directing its own formation through a dynamic covalent replication cycle. Additionally, the amine, formed by reduction of the replicating imine, is a more efficient catalyst for the formation of the replicating imine than the imine is a catalyst for its own formation.
| Original language | English |
|---|---|
| Pages (from-to) | 4589-4592 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 10 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 16 Oct 2008 |
Keywords
- VIRTUAL COMBINATORIAL LIBRARIES
- SYSTEMS CHEMISTRY
- SELF-REPLICATION
- THERMODYNAMIC CONTROL
- EFFECTIVE MOLARITIES
- AQUEOUS-SOLUTION
- SUBSTITUTION
- SELECTIVITY
- GENERATION
- CATALYSIS
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Dive into the research topics of 'Manipulating Replication Processes within a Dynamic Covalent Framework'. Together they form a unique fingerprint.Projects
- 1 Finished
-
EPSRC: PROBING CROSSCATALYSIS: Probing Crosscatalysis, Autocatalysis and Amplific
Philp, D. (PI)
1/01/07 → 31/07/10
Project: Standard
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