Synthesis of pure stereoisomers of benzo[b]thienyl dehydrophenylalanines by Suzuki cross-coupling. Preliminary studies of antimicrobial activity-Reference-Cited by-同舟云学术

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Synthesis of pure stereoisomers of benzo[b]thienyl dehydrophenylalanines by Suzuki cross-coupling. Preliminary studies of antimicrobial activity

Published:2004-12 Issue:51 Volume:60 Page:11821-11828
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Abreu Ana S.,Ferreira Paula M.T.,Monteiro Luís S.,Queiroz Maria-João R.P.,Ferreira Isabel C.F.R.,Calhelha Ricardo C.,Estevinho Letícia M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Tachykinin NK-1 receptor probed with constrained analogues of substance P

2. Synthesis and conformation of proline containing tripeptides constrained with phenylalanine-like aziridine and dehydrophenylalanine residues

3. A facile conversion of a 310 helical structure to a cyclic β-turn mimic in dehydrophenylalanine-derived small peptides through ring-closing metathesis

4. Dehydrophenylalanine analogues: conformational characterization

5. Michael addition of thiols, carbon nucleophiles and amines to dehydroamino acid and dehydropeptide derivativesElectronic supplementary information (ESI) available: experimental data for compounds 1–15. See http://www.rsc.org/suppdata/p1/b1/b106487h/

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