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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.

The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid Thumbnail


Authors

I.B. Masesane

J.A. Howard

R. Mondal



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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Copyright Statement
This is an Open Access article under the terms of the
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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