Synthesis of an Orthogonally-Protected Bifunctional Amino Acid for Conformationally Constrained Peptides
β Scribed by Martin J.I Andrews; Alethea B Tabor*
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 461 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The asymmetricsynthesisof (2s, 9R)-2,9-diaminodecanedioic acid, rnthogomllyprotectedfor incorporationinto cyclicpeptidesby solid-phasesynthesis,is described.
π SIMILAR VOLUMES
The synthesis of a series of novel (t-amino acids based on the nucleophilic substitution of protected 2-amino-4-bromobutanoic acid (1) is described. Basic, acidic or neutral amino acids can be obtained; chimerical amino acids carrying a coenzyme type structure in the side chain, multifunctional amin
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Conformationally constrained amino acid and dipeptide units can serve in mimics of specific secondary structures for studying relationships between peptide conformation and biological activity. A variety of mimics are required to study systematically the structure-activity relationships in biologica