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Iron-Mediated Photochemical Anti-Markovnikov Hydroazidation of Unactivated Olefins.

ABSTRACT: Unactivated olefins are converted to alkyl azides with bench-stable NaN₃ in the presence of FeCl₃·6H₂O under blue-light irradiation. The products are obtained with anti-Markovnikov selectivity, and the reaction can be performed under mild ambient conditions in the presence of air and moisture. The transformation displays broad functional group tolerance, which renders it suitable for functionalization of complex molecules. Mechanistic investigations are conducted to provide insight into the hydroazidation reaction and reveal the role of water from the iron hydrate as the H atom source.

SUBMITTER: Lindner H

PROVIDER: S-EPMC10591317 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

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Iron-Mediated Photochemical Anti-Markovnikov Hydroazidation of Unactivated Olefins.

Lindner Henry H Amberg Willi M WM Carreira Erick M EM

Journal of the American Chemical Society 20231009 41

Unactivated olefins are converted to alkyl azides with bench-stable NaN3 in the presence of FeCl3·6H2O under blue-light irradiation. The products are obtained with anti-Markovnikov selectivity, and the reaction can be performed under mild ambient conditions in the presence of air and moisture. The transformation displays broad functional group tolerance, which renders it suitable for functionalization of complex molecules. Mechanistic investigations are conducted ...[more]

PMID: 37811819

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