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Photo-Induced Homologation of Carbonyl Compounds for Iterative Syntheses.
Wang, Hua; Wang, Shun; George, Vincent; Llorente, Galder; König, Burkhard.
Afiliação
  • Wang H; Faculty of Chemistry and Pharmacy, University Regensburg, 93040, Regensburg, Germany.
  • Wang S; Department of Chemistry, School of Pharmacy, The Fourth Military Medical University, Xi'an, 710032, P. R. China.
  • George V; Faculty of Chemistry and Pharmacy, University Regensburg, 93040, Regensburg, Germany.
  • Llorente G; Faculty of Chemistry and Pharmacy, University Regensburg, 93040, Regensburg, Germany.
  • König B; Faculty of Chemistry and Pharmacy, University Regensburg, 93040, Regensburg, Germany.
Angew Chem Int Ed Engl ; 61(49): e202211578, 2022 12 05.
Article em En | MEDLINE | ID: mdl-36226924
ABSTRACT
We describe a photo-induced reaction for the in situ generation of highly reactive alkyl diazo species from carbonyl precursors via photo-excitation of N-tosylhydrazone anions. The diazo intermediates undergo efficient C-H insertion of aldehydes, leading to the productive synthesis of aldehydes and ketones. The method is applicable to the iterative synthesis of densely functionalized carbonyl compounds through sequential trapping of the diazo species with various aldehydes. The reaction proceeds without the need of any catalyst by light irradiation and features high functional group tolerance. More than 70 examples, some performed on a gram-scale, demonstrate the broad applicability of this reaction sequence in synthesis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldeídos / Cetonas Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldeídos / Cetonas Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha