Facultad de Farmacia
Centro
CLAUDIO
PALOMO NICOLAU
Investigador/a en el periodo 2000-2021
Publicaciones en las que colabora con CLAUDIO PALOMO NICOLAU (40)
2018
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α-Hydroxy Ketones as Masked Ester Donors in Brønsted Base Catalyzed Conjugate Additions to Nitroalkenes
Chemistry - A European Journal, Vol. 24, Núm. 15, pp. 3893-3901
2017
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β2, 2-Amino Acid N-Carboxyanhydrides Relying on Sequential Enantioselective C(4)-Functionalization of Pyrrolidin-2,3-diones and Regioselective Baeyer–Villiger Oxidation
Chemistry - A European Journal, Vol. 23, Núm. 34, pp. 8185-8195
2014
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Enantioselective construction of tetrasubstituted stereogenic carbons through brønsted base catalyzed michael reactions: α′-hydroxy enones as key enoate equivalent
Journal of the American Chemical Society, Vol. 136, Núm. 51, pp. 17869-17881
2013
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Catalytic enantioselective synthesis of tertiary thiols from 5h-thiazol-4-ones and nitroolefins: Bifunctional ureidopeptide-based brønsted base catalysis
Angewandte Chemie - International Edition, Vol. 52, Núm. 45, pp. 11846-11851
2012
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N-(diazoacetyl)oxazolidin-2-thiones as sulfur-donor reagents: Asymmetric synthesis of thiiranes from aldehydes
Angewandte Chemie - International Edition, Vol. 51, Núm. 43, pp. 10856-10860
2008
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Copper-catalyzed enantioselective conjugate addition of dialkylzinc reagents to α′-oxy enones
Chemistry - A European Journal, Vol. 14, Núm. 29, pp. 8768-8771
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
2003
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α′-hydroxy Enones as Achiral Templates for Lewis Acid-Catalyzed Enantioselective Diels - Alder Reactions
Journal of the American Chemical Society, Vol. 125, Núm. 46, pp. 13942-13943
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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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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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
1996
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Exo,exo-2,3-diaminoborneol-derived imidazolidinone as chiral auxiliary for asymmetric alkylations
Tetrahedron Letters, Vol. 37, Núm. 26, pp. 4565-4568
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New chiral acetate imide enolate for stereoselective aldol reactions
Tetrahedron Letters, Vol. 37, Núm. 38, pp. 6931-6934