Masesane, I.B. and Batsanov, A.S. and Howard, J.A. and Mondal, R. and Steel, P.G. (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).
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).
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|Publisher Web site:||http://dx.doi.org/10.1186/1860-5397-2-9|
|Publisher 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|
|Date accepted:||No date available|
|Date deposited:||23 May 2012|
|Date of first online publication:||May 2006|
|Date first made open access:||No date available|
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