Publicaciones en las que colabora con JESUS MARIA AIZPURUA IPARRAGUIRRE (18)

2005

  1. Synthesis of β-Amino Acids and Their Derivatives from β-Lactams: Update

    Enantioselective Synthesis of β-Amino Acids: Second Edition (John Wiley and Sons), pp. 477-495

2004

  1. Asymmetric synthesis of β-lactams through the Staudinger reaction and their use as building blocks of natural and nonnatural products

    Current Medicinal Chemistry, Vol. 11, Núm. 14, pp. 1837-1872

2001

  1. Diastereoselective Michael reactions of (1R)-(+)-camphor methyl ketone enolates with nitro olefins

    Tetrahedron Letters, Vol. 42, Núm. 29, pp. 4829-4831

  2. β-lactams as versatile intermediates in α- and β-amino acid synthesis

    Synlett, pp. 1813-1826

2000

  1. Versatility of β-lactams in synthesis. Studies directed toward the synthesis of complex nucleoside antibiotics and some macrocyclic peptides

    Pure and Applied Chemistry

1999

  1. Asymmetric synthesis of β-lactams by Staudinger ketene-imine cycloaddition reaction

    European Journal of Organic Chemistry

  2. From β-lactams to α- and β-amino acid derived peptides

    Amino Acids, Vol. 16, Núm. 3-4, pp. 321-343

  3. Highly diastereoselective aldol reactions with camphor-based acetate enolate equivalents

    Journal of Organic Chemistry, Vol. 64, Núm. 22, pp. 8193-8200

1997

  1. A contribution to the asymmetric synthesis of 3-amine β-lactams: The diastereoselective [2+2] cycloaddition reaction of chiral aminoketene equivalents with enolizable aldehyde-derived/mines

    Chemistry - A European Journal, Vol. 3, Núm. 9, pp. 1432-1441

1996

  1. A new and versatile procedure for the incorporation of α,β-diamino acids into peptides

    Chemical Communications, pp. 633-634

  2. A study on the asymmetric synthesis of β-lactams through double stereodifferentiating cycloaddition reactions

    Journal of Organic Chemistry, Vol. 61, Núm. 26, pp. 9186-9195

1995

  1. A mild method for the alcoholysis of β-lactams

    Tetrahedron Letters, Vol. 36, Núm. 49, pp. 9027-9030

1993

  1. Asymmetric synthesis of α-keto β-lactams via [2+2] cycloaddition reaction: A concise approach to optically active (α-hydroxy β-lactams and β-alkyl(aryl)isoserines.

    Tetrahedron Letters, Vol. 34, Núm. 39, pp. 6325-6328

1990

  1. Addition of α-bromoesters to azetidine-2,3-diones promoted by zinc-trimethylchlorosilane: a general synthesis of 3-trimethyisilyloxyazetidin-2-ones and α-alkylidene β-lactams.

    Tetrahedron Letters, Vol. 31, Núm. 44, pp. 6425-6428

  2. Highly stereoselective synthesis of α-hydroxy β-amino acids through β-lactams: application to the synthesis of the taxol and bestatin side chains and related systems.

    Tetrahedron Letters, Vol. 31, Núm. 44, pp. 6429-6432

  3. Tributyltin Hydride Addition to Nitroalkenes: A Convenient Procedure for the Conversion of Nitroalkenes into Nitroalkanes and Carbonyl Compounds

    Journal of Organic Chemistry, Vol. 55, Núm. 7, pp. 2070-2078

1987

  1. Reduction of α,β-unsaturated nitrocompounds with tributyltin hydride.

    Tetrahedron Letters, Vol. 28, Núm. 44, pp. 5365-5366

  2. The nef reaction on trialkylsilyl nitronates promoted by m-chloroper-benzoic acid. An efficient route to α-alkoxyketones from nitroalkanes.

    Tetrahedron Letters, Vol. 28, Núm. 44, pp. 5361-5364