A Crown Ozonide and its Rearrangement to a Macrocyclic Lactone

Research output: Contribution to journalArticleAcademicpeer-review

19 Citations (Scopus)
52 Downloads (Pure)

Abstract

The addition of singlet oxygen to 2,5-furo-18-crown-6 yields a crown ozonide, which rearranges quantitatively to a macrocyclic lactone.
Original languageEnglish
Pages (from-to)1443-1446
Number of pages4
JournalTetrahedron Letters
Volume22
Issue number15
DOIs
Publication statusPublished - 1981

Fingerprint

Dive into the research topics of 'A Crown Ozonide and its Rearrangement to a Macrocyclic Lactone'. Together they form a unique fingerprint.

Cite this