Facile synthesis of orthogonally protected amino acid building blocks for combinatorial N-backbone cyclic peptide chemistry

Journal of Peptide Research

Volumn 57, Issue 4, 2001, Pages 277-291

  Gellerman, G ^a   Elgavi, A ^a   Salitra, Y ^a   Kramer, M ^a  

^a Peptor Ltd   (Israel)

Author keywords

Biostability; Conformational constraint; Fmoc chemistry; N backbone cyclic peptides; Orthogonal protection; Reductive alkylation

Indexed keywords

ALDEHYDE; ALLYL COMPOUND; AMINO ACID; CARBONYL DERIVATIVE; CYCLOPEPTIDE; HALIDE; PEPTIDE DERIVATIVE; PROLINE; SCAPLS;

ALKYLATION; AMINATION; AMINO ACID SYNTHESIS; ARTICLE; COMBINATORIAL CHEMISTRY; CYCLIZATION; OPTICAL ROTATION; PARTIAL DRUG SYNTHESIS; PEPTIDE SYNTHESIS; PRIORITY JOURNAL; STRUCTURE ANALYSIS;

ALKYLATION; AMINO ACIDS; COMBINATORIAL CHEMISTRY TECHNIQUES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PEPTIDES, CYCLIC;

EID: 0034888722     PISSN: 1397002X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1397-002X.2000.0780.x     Document Type: Article

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