Laszlo Kurti
0000-0002-3412-5894
Harvard University
24 papers found
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Antimicrobial activity of a natural compound and analogs against multi-drug-resistant Gram-positive pathogens
Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines
Transition metal-free direct dehydrogenative arylation of activated C(sp3)–H bonds: synthetic ambit and DFT reactivity predictions
Symmetry in Cascade Chirality-Transfer Processes: A Catalytic Atroposelective Direct Arylation Approach to BINOL Derivatives
Scalable, Transition-Metal-Free Direct OximeO-Arylation: Rapid Access toO-Arylhydroxylamines and Substituted Benzo[b]furans
Rapid Synthesis of Fused N-Heterocycles by Transition-Metal-Free Electrophilic Amination of Arene CH Bonds
Aerobic, Transition-Metal-Free, Direct, and Regiospecific Mono-α-arylation of Ketones: Synthesis and Mechanism by DFT Calculations
Regiospecific Synthesis of Novel Cyclic Nitrostyrenes and 3-Substituted 2-Nitronaphthalenes
Organocatalytic Aryl–Aryl Bond Formation: An Atroposelective [3,3]-Rearrangement Approach to BINAM Derivatives
Transition-Metal-Free Direct Arylation: Synthesis of Halogenated 2-Amino-2′-hydroxy-1,1′-biaryls and Mechanism by DFT Calculations
Elusive Metal-Free Primary Amination of Arylboronic Acids: Synthetic Studies and Mechanism by Density Functional Theory
Enantioselective Aziridination of C=C
Formation of C-H Bonds
Formation of C-O Bonds
Cyclization
Formation of CC Bonds
Formation of CH Bonds
Planning Enantioselective Synthesis
Examples of Enantioselective Synthesis
Indole Diterpenoid Synthetic Studies. The Total Synthesis of (+)-Nodulisporic Acid F
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