Notice détaillée
Titre
LSYNC
Formal Name (French)
Laboratoire de synthese chimique
Formal Name (English)
Chemical Synthesis Laboratory
Lab Manager
Infoscience team
Group ID
U11423
Auteurs affilié
Gademann, Karl
Portmann, Cyril
Portmann, Cyril
Institut
ISIC
Faculté
SB
Note
Members of LSYNC-unit
Lien extérieur
http://lsync.epfl.ch
Publications
A biomimetic route to the peptide alkaloid anachelin
Highly enantio- and diastereoselective inverse electron demand hetero-Diels-Alder reaction
Highly enantioselective inverse-electron-demand hetero-Diels-Alder reactions of α,β-unsaturated aldehydes
Nostocarboline: isolation and synthesis of a new cholinesterase inhibitor from Nostoc 78-12A
Peptide folding induces high and selective affinity of a linear and small β-peptide to the human somatostatin receptor 4
Synthesis and Evaluation of the Bis-Nor-Anachelin Chromophore as Potential Cyanobacterial Ligand
The fourth helical secondary structure of β-peptides: The (P)-28-helix of a β-hexapeptide consisting of (2R,3S)-3-amino-2-hydroxy acid residues
The legendary Buergenstock 38th ESF/EUCHEM conference on stereochemistry: Buergenstock (Switzerland), April 26 to May 2, 2003
The peptide alkaloid Anachelin: NMR spectroscopic evidence for β-Turn formation in aqueous solution
Total Synthesis of Anachelin H
Voir toutes les publications (85)
Highly enantio- and diastereoselective inverse electron demand hetero-Diels-Alder reaction
Highly enantioselective inverse-electron-demand hetero-Diels-Alder reactions of α,β-unsaturated aldehydes
Nostocarboline: isolation and synthesis of a new cholinesterase inhibitor from Nostoc 78-12A
Peptide folding induces high and selective affinity of a linear and small β-peptide to the human somatostatin receptor 4
Synthesis and Evaluation of the Bis-Nor-Anachelin Chromophore as Potential Cyanobacterial Ligand
The fourth helical secondary structure of β-peptides: The (P)-28-helix of a β-hexapeptide consisting of (2R,3S)-3-amino-2-hydroxy acid residues
The legendary Buergenstock 38th ESF/EUCHEM conference on stereochemistry: Buergenstock (Switzerland), April 26 to May 2, 2003
The peptide alkaloid Anachelin: NMR spectroscopic evidence for β-Turn formation in aqueous solution
Total Synthesis of Anachelin H
Voir toutes les publications (85)
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