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Cyclic β-Peptoids
- Source :
- Organic Letters, Organic Letters, 2008, 10, pp.921-924, Organic Letters, American Chemical Society, 2008, 10, pp.921-924, HAL
- Publication Year :
- 2008
- Publisher :
- American Chemical Society (ACS), 2008.
-
Abstract
- The first synthesis of functionalized beta-peptoid macrocycles is reported. X-ray crystallographic structure of tetramer 9 reveals a C2-symmetrical derivative with unexpected all-cis-amide bonds and spatial disposition of the appendages toward the two opposite faces of the ring. Quantum calculations suggest that 9 is locked in this layout. These macrocycles constitute novel promising templates for multimeric ligation of biologically active ligands. The concept was exemplified by chemical decoration of tetramer 9 via "click" reactions.
- Subjects :
- [CHIM.ORGA]Chemical Sciences/Organic chemistry
Stereochemistry
Organic Chemistry
Stereoisomerism
Crystal structure
Ring (chemistry)
Biochemistry
Combinatorial chemistry
chemistry.chemical_compound
Protein structure
Template
chemistry
Tetramer
Physical and Theoretical Chemistry
Quantum
Derivative (chemistry)
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....e899f6386ac0a6a5ace46cabf2af7126