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Around isocyanide reactivity

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Around isocyanide reactivity

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Dearomatization of electron poor six-membered N-heterocycles through [3+2] annulation with aminocyclopropanes

α-Oxo-Ketenimines from Isocyanides and α-Haloketones: Synthesis and Divergent Reactivity

Switchable [3+2] and [4+2] Heteroannulation of Primary Propargylamines with Isonitriles to Imidazoles and 1,6-Dihydropyrimidines: Catalyst Loading Enabled Reaction Divergence

Total Synthesis of (±)-Strictamine

Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis

Carbon Dioxide Based N-Formylation of Amines Catalyzed by Fluoride and Hydroxide Anions

Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts

Rational Catalyst Design for Selective Hydrogenations

Atmospheric amines and ammonia measured with a chemical ionization mass spectrometer (CIMS)

Atmospheric amines and ammonia measured with a chemical ionization mass spectrometer (CIMS)

Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis

α-Oxo-Ketenimines from Isocyanides and α-Haloketones: Synthesis and Divergent Reactivity

Switchable [3+2] and [4+2] Heteroannulation of Primary Propargylamines with Isonitriles to Imidazoles and 1,6-Dihydropyrimidines: Catalyst Loading Enabled Reaction Divergence

Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts

Dearomatization of electron poor six-membered N-heterocycles through [3+2] annulation with aminocyclopropanes

Total Synthesis of (±)-Strictamine

Carbon Dioxide Based N-Formylation of Amines Catalyzed by Fluoride and Hydroxide Anions

Rational Catalyst Design for Selective Hydrogenations

Atmospheric amines and ammonia measured with a chemical ionization mass spectrometer (CIMS)

Atmospheric amines and ammonia measured with a chemical ionization mass spectrometer (CIMS)