Head-to-tail cyclization of linear oligoamides containing 4-benzylaminomethyl-1H-1,2,3-triazol-1-yl acetic acid monomers afforded a novel class of "extended macrocyclic peptoids". The identification of the conformation in solution for a cyclodimer and the X-ray crystal structure of a cyclic tetraamide are reported.
Macrocyclic Triazolopeptoids: A Promising Class of Extended Cyclic Peptoids
Araszczuk, Alicja MMembro del Collaboration Group
;D'Amato, AssuntaMembro del Collaboration Group
;Schettini, RosariaMembro del Collaboration Group
;Costabile, ChiaraMembro del Collaboration Group
;Della Sala, GiorgioMembro del Collaboration Group
;Pierri, GiovanniMembro del Collaboration Group
;Tedesco, ConsigliaMembro del Collaboration Group
;De Riccardis, FrancescoMembro del Collaboration Group
;Izzo, Irene
2022-01-01
Abstract
Head-to-tail cyclization of linear oligoamides containing 4-benzylaminomethyl-1H-1,2,3-triazol-1-yl acetic acid monomers afforded a novel class of "extended macrocyclic peptoids". The identification of the conformation in solution for a cyclodimer and the X-ray crystal structure of a cyclic tetraamide are reported.File in questo prodotto:
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