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Copper-catalyzed allylic substitution of nitroallyl derivatives with Grignard reagents

  • Laboratoire de Synthèse Organique
  • Queen Mary University of London

Research output: Contribution to journalArticlepeer-review

Abstract

Grignard reagents engage with nitroallyl derivatives in the presence of copper(i) salts to promote allylic substitution of the nitro group. The reaction is particularly effective with aryl Grignards and unsubstituted nitroallyl compounds but is also applicable to diversely substituted nitroallyl derivatives and both alkyl and vinyl Grignards. A mechanism involving a Cu(i)/Cu(iii) catalytic cycle is proposed for this transformation.

Original languageEnglish
Pages (from-to)6950-6953
Number of pages4
JournalChemical Communications
Volume62
Issue number26
DOIs
Publication statusPublished - 6 Mar 2026
Externally publishedYes

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