Makale
Tam Makale
Uluslararası
2018
Synthesis of Pyridazine and Pyrrole Analogues of 2-Aminotetralin as Potential Dopaminergics
Journal of Heterocyclic Chemistry
Cilt 55 · Sayı 6 · ss. 1489–1493 · 01.06.2018
Özet
Syntheses of pyridazine and pyrrole analogues of 2-aminotetralin starting from 3-cyclohexene-1-carboxylic acid are reported. All syntheses involve the following key steps: Curtius rearrangement for amine functionality, inverse electron demand Diels-Alder addition with 1,2,4,5-tetrazine for pyridazine ring synthesis, and pyridazine-to-pyrrole ring contraction for pyrrole ring formation.
Atıf için künye
Koçak, R., Daştan, A., & SARAÇOĞLU, N. (2018). Synthesis of Pyridazine and Pyrrole Analogues of 2-Aminotetralin as Potential Dopaminergics. Journal of Heterocyclic Chemistry, 55(6), 1489–1493. https://doi.org/10.1002/jhet.3180
BibTeX
@article{kocak2018-70710,
author = {Koçak, Ramazan and Daştan, Arif and SARAÇOĞLU, Nurullah},
title = {Synthesis of Pyridazine and Pyrrole Analogues of 2-Aminotetralin as Potential Dopaminergics},
journal = {Journal of Heterocyclic Chemistry},
year = {2018},
volume = {55},
number = {6},
pages = {1489--1493},
issn = {0022-152X},
doi = {10.1002/jhet.3180},
url = {https://akademik.atauni.edu.tr/yayinlar/70710-synthesis-of-pyridazine-and-pyrrole-analogues-of-2-aminotetralin-as-potential}
}