Regioselective Dearomative Amidoximation of Nonactivated Arenes Enabled by Photohomolytic Cleavage of N‐nitrosamides

PF Yuan, XT Huang, L Long, T Huang… - Angewandte Chemie …, 2024 - Wiley Online Library
Dearomative spirocyclization reactions represent a promising means to convert arenes into
three‐dimensional architectures; however, controlling the regioselectivity of radical …

Regioselective Dearomative Amidoximation of Nonactivated Arenes Enabled by Photohomolytic Cleavage of N‐nitrosamides

PF Yuan, XT Huang, L Long, T Huang… - Angewandte …, 2024 - Wiley Online Library
Dearomative spirocyclization reactions represent a promising means to convert arenes into
three‐dimensional architectures; however, controlling the regioselectivity of radical …

Regioselective Dearomative Amidoximation of Nonactivated Arenes Enabled by Photohomolytic Cleavage of N-nitrosamides.

PF Yuan, XT Huang, L Long, T Huang… - … (International ed. in …, 2024 - europepmc.org
Dearomative spirocyclization reactions represent a promising means to convert arenes into
three-dimensional architectures; however, controlling the regioselectivity of radical …

Regioselective Dearomative Amidoximation of Nonactivated Arenes Enabled by Photohomolytic Cleavage of N-nitrosamides

PF Yuan, XT Huang, L Long… - … (International ed. in …, 2024 - pubmed.ncbi.nlm.nih.gov
Dearomative spirocyclization reactions represent a promising means to convert arenes into
three-dimensional architectures; however, controlling the regioselectivity of radical …

Regioselective Dearomative Amidoximation of Nonactivated Arenes Enabled by Photohomolytic Cleavage of N‑nitrosamides

PF Yuan, XT Huang, L Long, T Huang… - Angewandte …, 2024 - ui.adsabs.harvard.edu
Dearomative spirocyclization reactions represent a promising means to convert arenes into
three‑dimensional architectures; however, controlling the regioselectivity of radical …