Claudio
Palomo Nicolau
Claudio Palomo Nicolau-rekin lankidetzan egindako argitalpenak (47)
2021
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Probing α-Amino Aldehydes as Weakly Acidic Pronucleophiles: Direct Access to Quaternary α-Amino Aldehydes by an Enantioselective Michael Addition Catalyzed by Brønsted Bases
Chemistry - A European Journal, Vol. 27, Núm. 7, pp. 2483-2492
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Synthesis of β-Hydroxy α-Amino Acids through Brønsted Base-Catalyzed syn-Selective Direct Aldol Reaction of Schiff Bases of Glycine o-Nitroanilide
Journal of Organic Chemistry, Vol. 86, Núm. 11, pp. 7757-7772
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syn-Selective Michael Reaction of α-Branched Aryl Acetaldehydes with Nitroolefins Promoted by Squaric Amino Acid Derived Bifunctional Brønsted Bases
European Journal of Organic Chemistry, Vol. 2021, Núm. 25, pp. 3604-3612
1993
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A Semiempirical Theoretical Study on the Formation of β-Lactams from Ketenes and Imines
Journal of the American Chemical Society, Vol. 115, Núm. 3, pp. 995-1004
1992
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Contribution to the Development of New Substitution Patterns of Optically Active β-Lactams: Synthesis of Homochiral 4-(1-Aminoalkyl)azetidin-2-ones from N-(tert-Butyloxycarbonyl) α-Amino Aldehyde-Derived Imines via Asymmetric Staudinger Reaction
Journal of the American Chemical Society, Vol. 114, Núm. 24, pp. 9360-9369
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Stereocontrolled synthesis of 3,5-dialkyl-4-amino pyrrolidin-2-ones from β-lactams as chiral templates.
Tetrahedron Letters, Vol. 33, Núm. 33, pp. 4827-4830
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Synthetic Aspects of Homochiral β‐Lactams Derived from N‐Protected α‐Aminoimines Via Asymmetric [2+2] Cycloaddition Reaction
Bulletin des Sociétés Chimiques Belges, Vol. 101, Núm. 7, pp. 541-554
1991
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A β-lactam approach to ψ-amino-β-keto acid derivatives.
Tetrahedron Letters, Vol. 32, Núm. 26, pp. 3115-3118
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Asymmetric synthesis of monocyclic β-lactams: application of imines derived from chiral N-protected α-amino aldehydes in the staudinger reaction
Tetrahedron Letters, Vol. 32, Núm. 26, pp. 3109-3110
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Oxidation of Alcohols Using Bis(trichloromethyl) Carbonate as Activator of Dimethyl Sulfoxide
Journal of Organic Chemistry
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Preparation of 3-Alkyl β-Lactams via the Ketene-Imine Cycloaddition Reaction Using α-(Phenylthio)alkanoyl Halides as Starting Materials: Application to the Synthesis of (±)-Carbapenem Building Blocks and Related Compounds
Journal of Organic Chemistry, Vol. 56, Núm. 14, pp. 4418-4428
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Preparation of chiral 3-unsubstituted β-lactams from 3-hydroxy β-lactams by using the alkoxyketene-imine cycloaddition reaction as an approach to the azetidinone ring: A formal synthesis of the carbapenem antibiotic (+)-PS-5.
Tetrahedron Letters, Vol. 32, Núm. 26, pp. 3105-3108
1990
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A New Version of the Peterson Olefination Using Bis(trimethylsilyl)methyl:Derivatives and Fluoride Ion as Catalyst
Journal of Organic Chemistry, Vol. 55, Núm. 8, pp. 2498-2503
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Alkyl(phenylthio)ketenes as synthetic equivalents of monoalkylketenes: a concise general route to 3-alkyl β-lactams as carbapenem buildings-blocks
Tetrahedron Letters
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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
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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
1989
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Alkyl(phenylthio)ketenes as synthetic equivalents of monoalkylketenes: A concise general route to 3-alkyl β-lactams as carbapenem building-blocks
Tetrahedron Letters, Vol. 30, Núm. 34, pp. 4577-4580
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The Reformatsky Type Reaction of Gilman and Speeter In The Preparation of Valuable β-lactams In Carbapenem Synthesis: Scope and Synthetic Utility
Journal of Organic Chemistry, Vol. 54, Núm. 24, pp. 5736-5745
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The α-bromoester-imine condensation promoted by zinc- trimethylchlorosilane: A stereospecific short formal synthesis of (±)-carbapenem antibiotics and related compounds
Journal of the Chemical Society, Chemical Communications
1988
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A short formal synthesis of the carbapenem antibiotic (±)-PS-5
Journal of the Chemical Society, Chemical Communications, pp. 809-810