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Publications by Francesco Tramutola
New Directing Groups for Metal-Catalyzed Asymmetric Carbon–Carbon Bond-Forming Processes: Stereoconvergent Alkyl–Alkyl Suzuki Cross-Couplings of Unactivated Electrophiles
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
New Heteroaryl Carbamates: Synthesis and Biological Screening in Vitro and in Mammalian Cells of Wild-Type and Mutant HIV-protease Inhibitors
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Related publications
Alkyl—Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature.
ChemInform
Silicon–Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles With Unactivated Secondary and Tertiary Alkyl Electrophiles
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating Between a CF3and an Alkyl Group
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Amino Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides, With Arylboronic Acids
Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides
Angewandte Chemie - International Edition
Catalysis
Chemistry
New Methods for Carbon-Nitrogen, Carbon-Sulfur, and Carbon-Carbon Bond Formations by Quinone-Mediated Oxidation-Reduction Condensation Using Alkyl Diphenylphosphinites
Proceedings of the Japan Academy Series B: Physical and Biological Sciences
Multidisciplinary
Biological Sciences
Medicine
Agricultural
Astronomy
Physics
Palladium-Catalyzed Decarbonylative Suzuki–Miyaura Cross-Coupling of Amides by Carbon–Nitrogen Bond Activation
Chemical Science
Chemistry
Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides With CO2
Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides With CO2
