Abstract
Synthesis of new octahydrodibenz[b,f]azepin-10-one derivatives by a two-step synthetic route based on 2-carbethoxymethyl cyclohexanone reactivity is reported.
Keywords: reductive amination, partially reduced dibenz[b,f]azepin-10-ones, cis/trans isomers
Letters in Organic Chemistry
Title: Efficient Synthesis of Octahydro-5H-Dibenz[b,f]azepin-10-one Derivatives by an Easy Two-Step Route from Available 2-Carbethoxymethyl Cyclohexanone and Anilines
Volume: 1 Issue: 3
Author(s): Alirio Palma, Jacqueline Jaime Barajas, Vladimir V. Kouznetsov, Elena Stashenko, Ali Bahsas and Juan Amaro-Luis
Affiliation:
Keywords: reductive amination, partially reduced dibenz[b,f]azepin-10-ones, cis/trans isomers
Abstract: Synthesis of new octahydrodibenz[b,f]azepin-10-one derivatives by a two-step synthetic route based on 2-carbethoxymethyl cyclohexanone reactivity is reported.
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Cite this article as:
Palma Alirio, Barajas Jaime Jacqueline, Kouznetsov V. Vladimir, Stashenko Elena, Bahsas Ali and Amaro-Luis Juan, Efficient Synthesis of Octahydro-5H-Dibenz[b,f]azepin-10-one Derivatives by an Easy Two-Step Route from Available 2-Carbethoxymethyl Cyclohexanone and Anilines, Letters in Organic Chemistry 2004; 1 (3) . https://dx.doi.org/10.2174/1570178043400767
DOI https://dx.doi.org/10.2174/1570178043400767 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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