An Investigation of the N-Arylsulfonylation of 2-Azetidinones

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)


N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield.
Original languageEnglish
JournalSynthetic Communications
Publication statusPublished - 1997


Dive into the research topics of 'An Investigation of the N-Arylsulfonylation of 2-Azetidinones'. Together they form a unique fingerprint.

Cite this