SÍNTESIS Y TRANSFORMACIÓN DE PRODUCTOS NATURALES EN COMPUESTOS BIOLÓGICAMENTE ACTIVOS. METODOLOGÍA SINTÉTICA CON AMIDUROS QUIRALES Y SULFONAS. ORGANOCATÁLISIS.
PRONABIOLACT
University of Oxford
Oxford, Reino UnidoPublicaciones en colaboración con investigadores/as de University of Oxford (10)
2006
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Asymmetric synthesis of pent-3-yl (R)-6-methyl-cyclohex-1-ene carboxylate
Tetrahedron Asymmetry, Vol. 17, Núm. 15, pp. 2183-2186
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Homochiral lithium amides for the asymmetric synthesis of β-amino acids
Tetrahedron Asymmetry, Vol. 17, Núm. 12, pp. 1793-1811
2005
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Cyclic β-amino acid derivatives: Synthesis via lithium amide promoted tandem asymmetric conjugate addition-cyclisation reactions
Organic and Biomolecular Chemistry, Vol. 3, Núm. 7, pp. 1284-1301
2004
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Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate
Organic and Biomolecular Chemistry, Vol. 2, Núm. 3, pp. 364-372
2003
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Preparation of methyl (1R,2S,5S)- and (1S,2R,5R)-2-amino-5-tert-butyl-cyclopentane-1-carboxylates by parallel kinetic resolution of methyl (RS)-5-tert-butyl-cyclopentene-1-carboxylate
Chemical Communications, Vol. 3, Núm. 19, pp. 2410-2411
1999
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Asymmetric synthesis of β-lactams and pseudopeptides via stereoselective conjugate additions of lithium (a-methylbenzyl)allylamide to ct,β-unsaturated iron acyl complexes
Journal of the Chemical Society - Perkin Transactions 1, pp. 3105-3110
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Conjugate addition to (α,β)(α,β)-diendioate esters by lithium (α- methylbenzyl)benzylamide: Tandem addition-cyclisation versus double addition
Tetrahedron Asymmetry, Vol. 10, Núm. 9, pp. 1637-1641
1997
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Asymmetric synthesis of (R)- and (S)-methyl (2-methoxycarbonylcyclopent-2-enyl)acetate and (R)- and (S)-2-(2-hydroxymethyl-cyclopent-2-enyl)ethanol
Tetrahedron Asymmetry, Vol. 8, Núm. 16, pp. 2683-2685
1995
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Labdane diterpenes from Halimium viscosum
Phytochemistry, Vol. 38, Núm. 3, pp. 663-666
1993
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Asymmetric syntheses of β-phenylalanine, α-methyl-β- phenylalanines and derivatives
Journal of the Chemical Society, Chemical Communications, pp. 1153-1155