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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

1
Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares and Departamento deQuímica Orgánica, Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain
2
Departamento de Química Orgánica, Facultad de Química, Pontificia Universidad Católica de Chile, 702843 Santiago de Chile, Chile
*
Author to whom correspondence should be addressed.
Presented at the 22nd International Electronic Conference on Synthetic Organic Chemistry, 15 November– 15 December 2018; Available Online: https://sciforum.net/conference/ecsoc-22.
Proceedings 2019, 9(1), 9; https://doi.org/10.3390/ecsoc-22-05767
Published: 14 November 2018
PDF [322 KB, uploaded 14 May 2019]
Note: In lieu of an abstract, this is an excerpt from the first page.

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1-Benzylisoquinolines are biogenetic precursors of a wide range of natural products of
pharmacological interest [...]
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
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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.

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