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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
Publisher Beilstein-Institut
Peer Reviewed Peer Reviewed
Volume 2
Issue 9
Article Number 9
DOI https://doi.org/10.1186/1860-5397-2-9

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Copyright Statement
This is an Open Access article under the terms of the<br /> Creative Commons Attribution License<br /> (http://creativecommons.org/licenses/by/2.0), which<br /> permits unrestricted use, distribution, and reproduction in<br /> any medium, provided the original work is properly cited.<br /> The license is subject to the Beilstein Journal of Organic<br /> Chemistry terms and conditions:<br /> (http://www.beilstein-journals.org/bjoc)<br /> The definitive version of this article is the electronic one<br /> which can be found at:<br /> doi:10.1186/1860-5397-2-9







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