Asymmetric Diels–Alder reaction using a new chiral β-nitroacrylate for enantiopure trans-β-norbornane amino acid preparation-Reference-Cited by-同舟云学术

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Asymmetric Diels–Alder reaction using a new chiral β-nitroacrylate for enantiopure trans-β-norbornane amino acid preparation

Published:2007-10 Issue:20 Volume:18 Page:2491-2496
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Calmès Monique,Escale Françoise,Didierjean Claude,Cazals Guillaume,Martinez Jean

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference45 articles.

1. Recent stereoselective synthetic approaches to β-amino acids

2. Enantioselective synthesis of β-aminoacids;Juaristi,1997

3. The Chemistry of 2-Aminocycloalkanecarboxylic Acids

4. Cyclic amino acid derivatives

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1. Progress in recent development of stereoselective synthesis of β2-amino acid derivatives from β-nitroacrylate derivatives;Organic & Biomolecular Chemistry;2020

2. Intermolecular Diels–Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide;The Journal of Organic Chemistry;2016-02-26

3. Bicyclic β-amino acids;Tetrahedron;2015-08

4. Cycloaddition of cyclohexa-2,4-dienones with β-nitroacrylates: a short and efficient entry into bicyclo[2.2.2]octanes endowed with β-nitro-ester and β-amino ester functionality;Tetrahedron Letters;2014-09

5. 3.8 Acetogenin (Polypriopionate) Derived Auxillaries: Hydroxyacid Derivatives;Comprehensive Chirality;2012

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