Issue 32, 2019

Synthesis of chiral nine and twelve-membered cyclic polyamines from natural building blocks

Abstract

A rational strategy for the facile and efficient cyclization of amino acid-based linear precursors forming nine and twelve-membered cyclic peptidomimetics is reported. The resulting chiral lactams can readily be reduced to substituted cyclic polyamine analogues of 1,4,7,10-tetraaza-cyclododecane (cyclen) and 1,4,7-triaza-cyclononane (TACN).

Graphical abstract: Synthesis of chiral nine and twelve-membered cyclic polyamines from natural building blocks

Supplementary files

Article information

Article type
Communication
Submitted
25 Jan 2019
Accepted
26 Mar 2019
First published
27 Mar 2019
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2019,55, 4715-4718

Synthesis of chiral nine and twelve-membered cyclic polyamines from natural building blocks

T. Müntener, F. Thommen, D. Joss, J. Kottelat, A. Prescimone and D. Häussinger, Chem. Commun., 2019, 55, 4715 DOI: 10.1039/C9CC00720B

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