Benito Alcaide spends much of his time researching Catalysis, Organic chemistry, Combinatorial chemistry, Allene and Stereochemistry. His study in Palladium, Ruthenium, Enantiopure drug, Stereoisomerism and Carbene falls under the purview of Catalysis. The concepts of his Combinatorial chemistry study are interwoven with issues in Lactam, Organocatalysis, Enantioselective synthesis, C c coupling and Stereoselectivity.
The various areas that Benito Alcaide examines in his Allene study include Elimination reaction, Cycloaddition, Alkene, Alkyne and Chemoselectivity. His Stereochemistry study integrates concerns from other disciplines, such as Molecule and Ring. His Ring research is multidisciplinary, incorporating elements of 2-Azetidinone and Reagent.
Benito Alcaide mainly investigates Organic chemistry, Stereochemistry, Catalysis, Medicinal chemistry and Combinatorial chemistry. His work on Lactam is typically connected to β lactams as part of general Stereochemistry study, connecting several disciplines of science. Benito Alcaide regularly ties together related areas like Reactivity in his Catalysis studies.
His work deals with themes such as Yield, Aryl and Nucleophile, which intersect with Medicinal chemistry. His Combinatorial chemistry study frequently draws connections to other fields, such as Moiety. Cycloaddition and Diels–Alder reaction is closely connected to Intramolecular force in his research, which is encompassed under the umbrella topic of Stereoselectivity.
Benito Alcaide mainly focuses on Catalysis, Organic chemistry, Combinatorial chemistry, Reactivity and Stereochemistry. The Catalysis study combines topics in areas such as Indole test, Metal and Medicinal chemistry. His work on Regioselectivity, Azetidine, Heteroatom and Homogeneous catalysis as part of general Organic chemistry research is frequently linked to Component, bridging the gap between disciplines.
The study incorporates disciplines such as Reagent, Surface modification and Synthon in addition to Combinatorial chemistry. His Reactivity study combines topics in areas such as Primary, Nucleophile and Density functional theory. His specific area of interest is Stereochemistry, where Benito Alcaide studies Lactam.
Catalysis, Organic chemistry, Reactivity, Regioselectivity and Stereochemistry are his primary areas of study. His Catalysis research includes themes of Combinatorial chemistry, Photochemistry, Metal and Medicinal chemistry. When carried out as part of a general Organic chemistry research project, his work on Nucleophile, Heteroatom, Cycloaddition and Azetidine is frequently linked to work in Component, therefore connecting diverse disciplines of study.
His Reactivity research includes elements of Hydroalkoxylation, Ring and Density functional theory. His biological study deals with issues like Allene, which deal with fields such as Lactam. Benito Alcaide combines subjects such as Enantiopure drug and Reaction mechanism with his study of Stereochemistry.
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β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products
Benito Alcaide;Pedro Almendros;Cristina Aragoncillo.
Chemical Reviews (2007)
Grubbs' ruthenium-carbenes beyond the metathesis reaction: less conventional non-metathetic utility.
Benito Alcaide;Pedro Almendros;Amparo Luna.
Chemical Reviews (2009)
Exploiting [2+2] cycloaddition chemistry: achievements with allenes
Benito Alcaide;Pedro Almendros;Cristina Aragoncillo.
Chemical Society Reviews (2010)
The Direct Catalytic Asymmetric Aldol Reaction
Benito Alcaide;Pedro Almendros.
European Journal of Organic Chemistry (2002)
β-Lactams as Versatile Synthetic Intermediates for the Preparation of Heterocycles of Biological Interest
Benito Alcaide;Pedro Almendros.
Current Medicinal Chemistry (2004)
4-Oxoazetidine-2-carbaldehydes as useful building blocks in stereocontrolled synthesis
Benito Alcaide;Pedro Almendros.
Chemical Society Reviews (2001)
Selective bond cleavage of the β-lactam nucleus: Application in stereocontrolled synthesis
Benito Alcaide;Pedro Almendros.
Synlett (2002)
Gold-catalyzed cyclization reactions of allenol and alkynol derivatives.
Benito Alcaide;Pedro Almendros.
Accounts of Chemical Research (2014)
Efficient entry to diversely functionalized spirocyclic oxindoles from isatins through carbonyl-addition/cyclization reaction sequences.
Benito Alcaide;Pedro Almendros;Raquel Rodríguez-Acebes.
Journal of Organic Chemistry (2006)
The direct catalytic asymmetric cross-aldol reaction of aldehydes.
Benito Alcaide;Pedro Almendros.
Angewandte Chemie (2003)
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