| Title |
Convenient synthesis of pyrazolo[4',3':5,6]pyrano[4,3-c][1,2]oxazoles via intramolecular nitrile oxide cycloaddition / |
| Authors |
Milišiūnaitė, Vaida ; Plytninkienė, Elena ; Bakšienė, Roberta ; Bieliauskas, Aurimas ; Krikštolaitytė, Sonata ; Račkauskienė, Greta ; Arbačiauskienė, Eglė ; Šačkus, Algirdas |
| DOI |
10.3390/molecules26185604 |
| Full Text |
|
| Is Part of |
Molecules.. Basel : MDPI. 2021, vol. 26, iss. 18, art. no. 5604, p. 1-18.. ISSN 1420-3049 |
| Keywords [eng] |
4-pyrazolaldoximes 1JCH ; fused ring systems ; intramolecular nitrile oxide cycloaddition ; isoxazole 15N NMR ; isoxazoline 15N NMR ; isoxazoline/isoxazole ; pyrazole |
| Abstract [eng] |
A simple and efficient synthetic route to the novel 3a,4-dihydro-3H,7H- and 4H,7H-pyrazolo[4',3':5,6]pyrano[4,3-c][1,2]oxazole ring systems from 3-(prop-2-en-1-yloxy)- or 3-(prop-2-yn-1-yloxy)-1H-pyrazole-4-carbaldehyde oximes has been developed by employing the intramolecular nitrile oxide cycloaddition (INOC) reaction as the key step. The configuration of intermediate aldoximes was unambiguously determined using NOESY experimental data and comparison of the magnitudes of 1JCH coupling constants of the iminyl moiety, which were greater by approximately 13 Hz for the predominant syn isomer. The structures of the obtained heterocyclic products were confirmed by detailed 1H, 13C and 15N NMR spectroscopic experiments and HRMS measurements. |
| Published |
Basel : MDPI |
| Type |
Journal article |
| Language |
English |
| Publication date |
2021 |
| CC license |
|
