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

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).

Detalles Bibliográficos
Autores principales: Masesane, Ishmael B, Batsanov, Andrei S, Howard, Judith A K, Mondal, Raju, Steel, Patrick G
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2006
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524792/
https://www.ncbi.nlm.nih.gov/pubmed/16674802
http://dx.doi.org/10.1186/1860-5397-2-9
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author Masesane, Ishmael B
Batsanov, Andrei S
Howard, Judith A K
Mondal, Raju
Steel, Patrick G
author_facet Masesane, Ishmael B
Batsanov, Andrei S
Howard, Judith A K
Mondal, Raju
Steel, Patrick G
author_sort Masesane, Ishmael B
collection PubMed
description 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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spelling pubmed-15247922006-07-29 The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid Masesane, Ishmael B Batsanov, Andrei S Howard, Judith A K Mondal, Raju Steel, Patrick G Beilstein J Org Chem Full Research Paper 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). Beilstein-Institut 2006-05-04 /pmc/articles/PMC1524792/ /pubmed/16674802 http://dx.doi.org/10.1186/1860-5397-2-9 Text en Copyright © 2006, Masesane et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://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: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Masesane, Ishmael B
Batsanov, Andrei S
Howard, Judith A K
Mondal, Raju
Steel, Patrick G
The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title_full The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title_fullStr The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title_full_unstemmed The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title_short The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
title_sort oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524792/
https://www.ncbi.nlm.nih.gov/pubmed/16674802
http://dx.doi.org/10.1186/1860-5397-2-9
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