Resumen: α‐Brominated ketones and aldehydes, with two adjacent electrophilic carbon atoms, are highly valuable synthetic intermediates in organic synthesis, however, their synthesis from unsymmetrical ketones is very challenging, and current methods suffer from low selectivity. We present a new, reliable, and efficient method for the synthesis of α‐bromocarbonyl compounds in excellent yields and with excellent selectivities. Starting from allylic alcohols as the carbonyl precursors, the combination of a 1,3‐hydrogen shift catalyzed by iridium(III) with an electrophilic bromination gives α‐bromoketones and aldehydes in good to excellent yields. The selectivity of the process is determined by the structure of the starting allylic alcohol; thus, α‐bromoketones formally derived from unsymmetrical ketones can be synthesized in a straightforward and selective manner. Idioma: Inglés DOI: 10.1002/chem.201402350 Año: 2014 Publicado en: Chemistry - A European Journal 20, 34 (2014), 10703-10709 ISSN: 0947-6539 Factor impacto JCR: 5.731 (2014) Categ. JCR: CHEMISTRY, MULTIDISCIPLINARY rank: 22 / 154 = 0.143 (2014) - Q1 - T1 Tipo y forma: Article (Published version)
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