N -acylsulfonamide assisted tandem C-H olefination/annulation: Synthesis of isoindolinones

Chen Zhu, J R Falck

Research output: Contribution to journalArticle

119 Scopus citations

Abstract

A tandem C-H olefination/annulation sequence directed by N-acylsulfonamides affords a variety of isoindolinones. This transformation is compatible with aliphatic alkenes as well as conjugated alkenes. Notably, molecular oxygen can be used as the sole, eco-friendly oxidant.(Figure Presented)

Original languageEnglish (US)
Pages (from-to)1214-1217
Number of pages4
JournalOrganic Letters
Volume13
Issue number5
DOIs
StatePublished - Mar 4 2011

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Fingerprint Dive into the research topics of 'N -acylsulfonamide assisted tandem C-H olefination/annulation: Synthesis of isoindolinones'. Together they form a unique fingerprint.

  • Cite this