Publicaciones en colaboración con investigadoras/es de University of Zurich (11)

2013

  1. Chirality-driven folding of short β-lactam pseudopeptides

    Journal of Organic Chemistry, Vol. 78, Núm. 2, pp. 224-237

2006

  1. Functionalization of N-[(silyl)methyl]-β-lactam carbanions with carbon electrophiles

    Journal of Organic Chemistry, Vol. 71, Núm. 17, pp. 6368-6373

2004

  1. Synthesis of type II β-turn surrogate dipeptides based on syn-α-amino-α,β-dialkyl-β-lactams

    Organic Letters, Vol. 6, Núm. 24, pp. 4443-4446

2003

  1. Development of a New Family of Conformationally Restricted Peptides as Potent Nucleators of β-Turns. Design, Synthesis, Structure, and Biological Evaluation of β-Lactam Peptide Analogue of Melanostatin

    Journal of the American Chemical Society, Vol. 125, Núm. 52, pp. 16243-16260

2001

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

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

2000

  1. On the question of the diastereoselective alkylation of 4-unsubstituted 3-amino β-lactams. A concise synthesis of α-branched α-amino β-lactams and their coupling with α-amino acid esters

    Tetrahedron

1999

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

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

  2. α-alkyl-α-amino-β-lactam peptides: Design, synthesis, and conformational features

    Angewandte Chemie - International Edition, Vol. 38, Núm. 20, pp. 3056-3058

1997

  1. Construction of quaternary stereogenic centers via [2 + 2] cycloaddition reactions. Synthesis of homochiral 4,4-disubstituted 2-azetidinones and imine substituent effects on β-lactam formation

    Journal of Organic Chemistry, Vol. 62, Núm. 7, pp. 2070-2079

1996

  1. 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

  2. Generation of threonine- and azathreonine N-carboxy anhydrides from α-hydroxy β-lactams promoted by 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) in combination with sodium hypochlorite

    Journal of Organic Chemistry, Vol. 61, Núm. 13, pp. 4400-4404