<p> Disclosed herein is a metal-free, photochemical strategy for the direct alkylation of indoles. The reaction, which occurs at ambient temperature, is driven by the photochemical activity of electron donor-acceptor (EDA) complexes, generated upon association of substituted 1H-indoles with electron-accepting benzyl and phenacyl bromides. Significant mechanistic insights are provided by the X-ray single-crystal analysis of an EDA complex relevant to the photo-alkylation and the determination of the quantum yield (Φ) of the process.</p>
Inglés
alkylation; indoles; photochemistry; radical; synthetic methods
Wiley
Angew. Chem. Int. Ed.
SEV-2013-0319, 278541
MINECO
ERC
Severo Ochoa Excellence Accreditation 2014-2018, Starting Grant,
ORGA-NAUT,
©2015Wiley-KH Kerlag GmbH&Co. KGaA, Weinheim
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