Literature DB >> 21968501

New 1,3-amino alcohols derived from enantiopure bridgehead β-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acids.

Christophe André1, Monique Calmès, Françoise Escale, Muriel Amblard, Jean Martinez, Olivier Songis.   

Abstract

Constrained enantiopure bicyclic β-amino acids derived from the asymmetric Diels-Alder reaction of the (R)-benzyl-4-(3-acryloyloxy-4,4-dimethyl-2-oxopyrrolidin-1-yl)-benzoate and the 1-(benzyloxycarbonylamino)cyclohexadiene provide original templates for the construction of new rigid enantiopure 1,3-amino alcohols.

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Year:  2011        PMID: 21968501     DOI: 10.1007/s00726-011-1097-6

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  2 in total

1.  Conformational analysis and intramolecular hydrogen bonding of cis-3-aminoindan-1-ol: a quantum chemical study.

Authors:  Djaffar Kheffache; Hind Guemmour; Azzedine Dekhira; Ahmed Benaboura; Ourida Ouamerali
Journal:  J Mol Model       Date:  2013-09-13       Impact factor: 1.810

2.  Syntheses of four enantiomers of 2,3-diendo- and 3-endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic acid and their saturated analogues.

Authors:  Márta Palkó; Mikko M Hänninen; Reijo Sillanpää; Ferenc Fülöp
Journal:  Molecules       Date:  2013-12-06       Impact factor: 4.411

  2 in total

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