Facultad de Farmacia
Centro
University of Zurich
Zúrich, SuizaPublicaciones en colaboración con investigadoras/es de University of Zurich (21)
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Healthy and diseasedin vitromodels of vascular systems
Lab on a Chip, Vol. 21, Núm. 4, pp. 641-659
2016
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Nuclear phosphoproteomic screen uncovers ACLY as mediator of IL-2-induced proliferation of CD4+ T lymphocytes
Molecular and Cellular Proteomics, Vol. 15, Núm. 6, pp. 2076-2092
2014
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A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Forensic Science International: Genetics, Vol. 12, pp. 12-23
2008
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Detection of clinical biomarkers using a novel parabolic microchip diagnostic platform
Technical Proceedings of the 2008 NSTI Nanotechnology Conference and Trade Show, NSTI-Nanotech, Nanotechnology 2008
2005
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Asymmetric propionate aldol reactions of a chiral lithium enolate accessible from direct enolization with n-butyllithium
Arkivoc, Vol. 2005, Núm. 6, pp. 377-392
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Lewis acid catalyzed asymmetric cycloadditions of nitrones: α′-hydroxy enones as efficient reaction partners
Angewandte Chemie - International Edition, Vol. 44, Núm. 38, pp. 6187-6190
2004
2002
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A chiral acrylate equivalent for metal-free Diels-Alder reactions: endo-2-acryloylisoborneol
Journal of the American Chemical Society, Vol. 124, Núm. 35, pp. 10288-10289
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Design and synthesis of a novel class of sugar-peptide hybrids: C-linked glyco β-amino acids through a stereoselective "acetate" Mannich reaction as the key strategic element
Journal of the American Chemical Society, Vol. 124, Núm. 29, pp. 8637-8643
2001
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(2S*,3R*,4S*,5R*)-3-(S*-1-Benzyloxyethyl)-4-methyl-4-nitro-5-phenylproline methyl ester
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, Vol. 57
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Alkylation of chiral α-hydroxy ketones derived from (1R)-(+)-camphor. An asymmetric variant of the classical acetylene route to carbonyl compounds
Organic Letters, Vol. 3, Núm. 21, pp. 3249-3252
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Diastereoselective Michael reactions of (1R)-(+)-camphor methyl ketone enolates with nitro olefins
Tetrahedron Letters, Vol. 42, Núm. 29, pp. 4829-4831
2000
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Camphor-based α-bromo ketones for the asymmetric Darzens reaction
Journal of Organic Chemistry, Vol. 65, Núm. 26, pp. 9007-9012
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Origins of the loss of concertedness in pericyclic reactions: Theoretical prediction and direct observation of stepwise mechanisms in [3 + 2] thermal cycloadditions
Journal of the American Chemical Society, Vol. 122, Núm. 25, pp. 6078-6092
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α-Oxymethyl ketone enolates for the asymmetric Mannich reaction. From acetylene and N-alkoxycarbonylimines to β-amino acids
Angewandte Chemie - International Edition, Vol. 39, Núm. 6, pp. 1063-1066
1999
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Highly diastereoselective aldol reactions with camphor-based acetate enolate equivalents
Journal of Organic Chemistry, Vol. 64, Núm. 22, pp. 8193-8200
1998
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Design and Evaluation of a Practical Camphor-Based Methyl Ketone Enolate for Highly Stereoselective "Acetate" Aldol Reactions
Angewandte Chemie - International Edition, Vol. 37, Núm. 1-2, pp. 180-182
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Stereocontrolled Synthesis of Highly Substituted Proline Esters via [3 + 2] Cycloaddition between N-Metalated Azomethine Ylides and Nitroalkenes. Origins of the Metal Effect on the Stereochemical Outcome
Journal of Organic Chemistry, Vol. 63, Núm. 6, pp. 1795-1805
1996
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New chiral acetate imide enolate for stereoselective aldol reactions
Tetrahedron Letters, Vol. 37, Núm. 38, pp. 6931-6934