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

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).

SUBMITTER: Masesane IB

PROVIDER: S-EPMC1524792 | biostudies-literature | 2006 May

REPOSITORIES: biostudies-literature

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

Masesane Ishmael B IB Batsanov Andrei S AS Howard Judith A K JA Mondal Raju R Steel Patrick G PG

Beilstein journal of organic chemistry 20060504

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). ...[more]

PMID: 16674802

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