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

Beilstein Journal of Organic Chemistry (2006) 2
DOI: 10.1186/1860-5397-2-9
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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). © 2006 Masesane et al; licensee Beilstein-Institut.

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APA

Masesane, I. B., Batsanov, A. S., Howard, J. A. K., Mondal, R., & 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. https://doi.org/10.1186/1860-5397-2-9

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