Abstract
A set of macrocycles was generated by solid phase synthesis of linear trimers of 5-aminoacyl-3-aminomethyl-benzoates followed by resin cleavage and solution phase macrocyclization. These scaffolds can serve as useful building blocks for molecular recognition studies, especially where differentially functionalized molecular platforms spanning large surface areas are required.
Original language | English (US) |
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Pages (from-to) | 2787-2789 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 50 |
Issue number | 23 |
DOIs | |
State | Published - Jun 10 2009 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry