Tetrahydro-4H-(pyrrolo[3,4-d]isoxazol-3-yl)methanamine scaffold was designed as diamino derivative to stabilize parallel turn conformations. Its synthesis took advantage of a [1,3]-dipolar cycloaddition reaction between the nitrile oxide derived from the inexpensive enantiopure L-phenylalanine, and N-benzyl-3-pyrroline. Two diastereoisomers were formed whose distribution depends on the selected base. 3aR,6aS-Isomer is favoured in organic bases which formation is driven by pi-interactions. On the other hand, the above interactions were significantly prevented using an inorganic base due to the chaotropic effect of the cation, decreasing the amount of the above isomer. Finally, we demonstrated that this isomer is able of stabilizing parallel turn conformations when inserted in short peptide sequences.
|Titolo:||Tetrahydro-4H-(pyrrolo[3,4-d]isoxazol-3-yl)methanamine : a bicyclic diamino scaffold stabilizing parallel turn conformations|
GELMI, MARIA LUISA (Corresponding)
|Parole Chiave:||[1,3]-dipolar cycloaddition; peptidomimetic; parallel turn conformation|
|Settore Scientifico Disciplinare:||Settore CHIM/06 - Chimica Organica|
|Data di pubblicazione:||ott-2018|
|Digital Object Identifier (DOI):||10.1021/acs.joc.8b01299|
|Appare nelle tipologie:||01 - Articolo su periodico|