Rearrangement of 3-(4,5-dimethoxy -2-vinylphenyl)-2-methyl -5-nitroisoquinolin-1(2H)-one to 2-(6,7-dimethoxy-1-oxoisoquinolin -2(1H)-yl)-N-methylbenzamide: A Mechanistic Proposal †
Excerpt
1-Benzylisoquinolines are biogenetic precursors of a wide range of natural products of
pharmacological interest [...]
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Treus, M.; Salas, C.O.; Estévez, J.C.; Tapia, R.A.; Estévez, R.J. Rearrangement of 3-(4,5-dimethoxy -2-vinylphenyl)-2-methyl -5-nitroisoquinolin-1(2H)-one to 2-(6,7-dimethoxy-1-oxoisoquinolin -2(1H)-yl)-N-methylbenzamide: A Mechanistic Proposal. Proceedings 2019, 9, 9. https://doi.org/10.3390/ecsoc-22-05767
Treus M, Salas CO, Estévez JC, Tapia RA, Estévez RJ. Rearrangement of 3-(4,5-dimethoxy -2-vinylphenyl)-2-methyl -5-nitroisoquinolin-1(2H)-one to 2-(6,7-dimethoxy-1-oxoisoquinolin -2(1H)-yl)-N-methylbenzamide: A Mechanistic Proposal. Proceedings. 2019; 9(1):9. https://doi.org/10.3390/ecsoc-22-05767
Chicago/Turabian StyleTreus, Mónica, Cristian O. Salas, Juan C. Estévez, Ricardo A. Tapia, and Ramón J. Estévez. 2019. "Rearrangement of 3-(4,5-dimethoxy -2-vinylphenyl)-2-methyl -5-nitroisoquinolin-1(2H)-one to 2-(6,7-dimethoxy-1-oxoisoquinolin -2(1H)-yl)-N-methylbenzamide: A Mechanistic Proposal" Proceedings 9, no. 1: 9. https://doi.org/10.3390/ecsoc-22-05767