Journal
ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 11, Issue 1, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202100640
Keywords
Alkyl radical; Borate complex; Direct photoexcitation; Minisci reaction
Categories
Funding
- JSPS KAKENHI [JP21H04681, JP17H06449, JP21K06474]
- Kanazawa University SAKIGAKE project 2020
- JST, PRESTO [JPMJPR19T2]
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The photoexcitable borate enables Minisci C-H alkylation of heteroarenes, providing a clean system using alkylborate, O-2, and visible light. Direct photoexcitation of alkylborate generates tertiary, secondary, and primary-alkyl radicals, including methyl radicals, offering a choice for the functionalization of heteroarenes.
The photoexcitable borate enabling Minisci C-H alkylation of heteroarene has been described. This protocol using alkylborate only needed O-2 and visible light, which provides a considerably clean system. The direct photoexcitation of alkylborate allowed the generation of tertiary, secondary, and primary-alkyl radical including methyl radical. This light-driven Minisci reaction gave a choice for the functionalization of heteroarenes.
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