Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes

Sangwon Seo, Ming Gao, Eva Paffenholz, Michael C. Willis

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

We demonstrate that aryltriazenes can promote three distinctive types of C-H functionalization reactions, allowing the preparation of complex benzene molecules with diverse substitution patterns. 2-Triazenylbenzaldehydes are shown to be efficient substrates for Rh(I)-catalyzed intermolecular alkyne hydroacylation reactions. The resulting triazene-substituted ketone products can then undergo either a Rh(III)-catalyzed C-H activation, or an electrophilic aromatic substitution reaction, achieving multifunctionalization of the benzene core. Subsequent triazene derivatization provides traceless products.

Original languageEnglish
Pages (from-to)6091-6098
Number of pages8
JournalACS Catalysis
Volume11
Issue number10
DOIs
StatePublished - 21 May 2021

Bibliographical note

Publisher Copyright:
©

Keywords

  • benzene
  • hydroacylation
  • rhodium
  • sequential catalysis
  • triazene

Fingerprint

Dive into the research topics of 'Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes'. Together they form a unique fingerprint.

Cite this