The scientist’s investigation covers issues in Cycloaddition, Organic chemistry, Nitrone, Stereochemistry and Enantiopure drug. Alberto Brandi interconnects Dendrimer, Intramolecular force, Lentiginosine, Adduct and Total synthesis in the investigation of issues within Cycloaddition. In the subject of general Organic chemistry, his work in Reagent, Catalysis and Methylene is often linked to β lactams, thereby combining diverse domains of study.
Alberto Brandi combines subjects such as Bicyclic molecule, Medicinal chemistry, Regioselectivity, 1,3-Dipolar cycloaddition and Stereoselectivity with his study of Nitrone. He has researched Stereochemistry in several fields, including Stereocenter, Enantioselective synthesis and Stereoisomerism. His work deals with themes such as Mitsunobu reaction, Pyrroline and Hastanecine, which intersect with Enantiopure drug.
Alberto Brandi mainly investigates Stereochemistry, Organic chemistry, Cycloaddition, Nitrone and Enantiopure drug. His Stereochemistry study incorporates themes from Ring and Stereoselectivity. His Polymer chemistry research extends to the thematically linked field of Organic chemistry.
His research investigates the link between Cycloaddition and topics such as Indolizidine that cross with problems in Indolizidines. His studies deal with areas such as Kinetic resolution, Stereocenter, 1,3-Dipolar cycloaddition, Nitrile and Asymmetric induction as well as Nitrone. His Enantiopure drug study frequently draws connections to adjacent fields such as Pyrroline.
Alberto Brandi focuses on Organic chemistry, Stereochemistry, Cycloaddition, Medicinal chemistry and Nanotechnology. His research brings together the fields of Enantiopure drug and Stereochemistry. His Enantiopure drug study combines topics in areas such as Nitrone, Racemic mixture and Crystallography.
His Cycloaddition study combines topics from a wide range of disciplines, such as Photochemistry, Wittig reaction and Rhodium. His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Indolizidines, Indolizidine, Methanol and Addition reaction. His Pyrroline research includes elements of Amino acid, Alkyne, Ring and Stereoselectivity.
His primary areas of investigation include Stereochemistry, Carbon nanotube, Cycloaddition, Organic chemistry and Yield. His Stereochemistry research incorporates themes from Amino acid and Enantiopure drug. He has included themes like Pyrrolidine, Trifluoroacetic acid, Nitrone, Peptidomimetic and Stereoselectivity in his Enantiopure drug study.
The Carbon nanotube study combines topics in areas such as Nanoparticle, Transmission electron microscopy and Click chemistry. Alberto Brandi interconnects Iminium and Surface modification in the investigation of issues within Cycloaddition. His research investigates the connection with Yield and areas like Indolizidine which intersect with concerns in Medicinal chemistry.
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Heterocycles from alkylidenecyclopropanes.
Alberto Brandi;Stefano Cicchi;Franca M Cordero;Andrea Goti.
Chemical Reviews (2003)
Novel syntheses of azetidines and azetidinones.
Alberto Brandi;Stefano Cicchi;Franca M. Cordero.
Chemical Reviews (2008)
Synthesis of Methylene- and Alkylidenecyclopropane Derivatives.
Alberto Brandi;Andrea Goti.
Chemical Reviews (1998)
1,3-Aminoalcohols by reductive cleavage of isoxazolidines with molybdenum hexacarbonyl
Stefano Cicchi;Andrea Goti;Alberto Brandi;Antonio Guarna.
Tetrahedron Letters (1990)
Stereocontrolled Cyclic Nitrone Cycloaddition Strategy for the Synthesis of Pyrrolizidine and Indolizidine Alkaloids
Alberto Brandi;Francesca Cardona;Stefano Cicchi;Franca M. Cordero.
Chemistry: A European Journal (2009)
Assignment of the Absolute Configuration of Natural Lentiginosine by Synthesis and Enzymic Assays of Optically Pure (+) and (-)-Enantiomers
Alberto Brandi;Stefano Cicchi;Franca M. Cordero;Roberta Frignoli.
Journal of Organic Chemistry (1995)
Progress in the synthesis and transformations of alkylidenecyclopropanes and alkylidenecyclobutanes.
Alberto Brandi;Stefano Cicchi;Franca M. Cordero;Andrea Goti.
Chemical Reviews (2014)
A Five-Membered Enantiopure Cyclic Nitrone from Malic Acid by Regioselective Oxidation of Cyclic Hydroxylamine. Synthesis of (1S,7S,8aR)-Octahydro-1,7-dihydroxyindolizine
Stefano Cicchi;Andrea Goti;Alberto Brandi.
Journal of Organic Chemistry (1995)
Manganese dioxide oxidation of hydroxylamines to nitrones
Stefano Cicchi;Marco Marradi;Andrea Goti;Alberto Brandi.
Tetrahedron Letters (2001)
New synthesis of five-membered cyclic nitrones from tartaric acid
Stefano Cicchi;Ingeborg Hold;Alberto Brandi.
Journal of Organic Chemistry (1993)
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