I.B. Masesane
The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
Masesane, I.B.; Batsanov, A.S.; Howard, J.A.; Mondal, R.; Steel, P.G.
Authors
Dr Andrei Batsanov a.s.batsanov@durham.ac.uk
Academic Visitor
J.A. Howard
R. Mondal
Professor Patrick Steel p.g.steel@durham.ac.uk
Professor
Abstract
The nitro oxanorbornene adduct derived from the Diels-Alder reaction of ethyl (E)-3-nitroacrylate and furan provides a versatile template for the stereoselective synthesis of hydroxylated derivatives of 2-aminocyclohexanecarboxylic acid (ACHC).
Citation
Masesane, I., Batsanov, A., Howard, J., Mondal, R., & Steel, P. (2006). The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid. Beilstein Journal of Organic Chemistry, 2(9), Article 9. https://doi.org/10.1186/1860-5397-2-9
Journal Article Type | Article |
---|---|
Publication Date | 2006 |
Deposit Date | May 23, 2012 |
Publicly Available Date | May 23, 2012 |
Journal | Beilstein Journal of Organic Chemistry |
Print ISSN | 1860-5397 |
Electronic ISSN | 1860-5397 |
Publisher | Beilstein-Institut |
Peer Reviewed | Peer Reviewed |
Volume | 2 |
Issue | 9 |
Article Number | 9 |
DOI | https://doi.org/10.1186/1860-5397-2-9 |
Public URL | https://durham-repository.worktribe.com/output/1543336 |
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Creative Commons Attribution License
(http://creativecommons.org/licenses/by/2.0), which
permits unrestricted use, distribution, and reproduction in
any medium, provided the original work is properly cited.
The license is subject to the Beilstein Journal of Organic
Chemistry terms and conditions:
(http://www.beilstein-journals.org/bjoc)
The definitive version of this article is the electronic one
which can be found at:
doi:10.1186/1860-5397-2-9
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