Abstract
A novel synthetic route has been developed for the preparation of pharmacologically remarkable (R)- (-)-2-methoxyapomorphine (2) and other 2-alkoxyapomorphines 8-10.
Keywords: 2-Alkoxyapomorphines, oripavine, acid-catalyzed rearrangement, O-demethylation, dopamine receptor binding affinity
Letters in Organic Chemistry
Title: New and Efficient Synthesis of 2-Alkoxyapomorphines
Volume: 4 Issue: 1
Author(s): Sandor Berenyi, Csaba Csutoras, Attila Sipos and Zsuzsanna Gyulai
Affiliation:
Keywords: 2-Alkoxyapomorphines, oripavine, acid-catalyzed rearrangement, O-demethylation, dopamine receptor binding affinity
Abstract: A novel synthetic route has been developed for the preparation of pharmacologically remarkable (R)- (-)-2-methoxyapomorphine (2) and other 2-alkoxyapomorphines 8-10.
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Cite this article as:
Berenyi Sandor, Csutoras Csaba, Sipos Attila and Gyulai Zsuzsanna, New and Efficient Synthesis of 2-Alkoxyapomorphines, Letters in Organic Chemistry 2007; 4 (1) . https://dx.doi.org/10.2174/157017807780037397
DOI https://dx.doi.org/10.2174/157017807780037397 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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