Solid-phase synthesis of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones via a cyclization/release strategy

A solid-phase synthesis procedure for the parallel preparation of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones is described. The methodology applies alpha- and alicyclic beta-amino acid building blocks to construct the seven-membered heterocyclic core, while alcohols are used for further skeletal...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Caroen Jurgen
Clemmen An
Kámán Judit
Backaert Fréderique
Goeman Jan L.
Fülöp Ferenc
Van der Eycken Johan
Dokumentumtípus: Cikk
Megjelent: 2016
Sorozat:TETRAHEDRON 72 No. 1
doi:10.1016/j.tet.2015.11.023

mtmt:3005721
Online Access:http://publicatio.bibl.u-szeged.hu/12634
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520 3 |a A solid-phase synthesis procedure for the parallel preparation of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones is described. The methodology applies alpha- and alicyclic beta-amino acid building blocks to construct the seven-membered heterocyclic core, while alcohols are used for further skeletal decoration. The use of a cyclization/release strategy permits the isolation of the target cyclic alpha,beta-dipeptides in good crude purities and generally moderate to good yields. A 26-membered model library is reported and NMR spectroscopical data are used to describe the overall conformational behaviour of the obtained homodiketopiperazines. (C) 2015 Elsevier Ltd. All rights reserved. 
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700 0 1 |a Kámán Judit  |e aut 
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700 0 2 |a Van der Eycken Johan  |e aut 
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