Issue 7, 2014

Ugi 4-CR synthesis of γ- and δ-lactams providing new access to diverse enzyme interactions, a PDB analysis

Abstract

A three step synthesis of N-unsubstituted tetrazolo γ- and δ-lactams involving a key Ugi-4CR is presented. The compounds, otherwise difficult to access, are conveniently synthesized in overall good yields by our route. PDB analysis of the N-unsubstituted γ- and δ-lactam fragment reveals a strongly tri-directional hydrogen bond donor acceptor interaction with the amino acids of the binding sites.

Graphical abstract: Ugi 4-CR synthesis of γ- and δ-lactams providing new access to diverse enzyme interactions, a PDB analysis

Supplementary files

Article information

Article type
Concise Article
Submitted
08 Apr 2014
Accepted
13 May 2014
First published
14 May 2014

Med. Chem. Commun., 2014,5, 949-952

Author version available

Ugi 4-CR synthesis of γ- and δ-lactams providing new access to diverse enzyme interactions, a PDB analysis

A. Boltjes, G. P. Liao, T. Zhao, E. Herdtweck and A. Dömling, Med. Chem. Commun., 2014, 5, 949 DOI: 10.1039/C4MD00162A

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