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An unusual and highly efficient access to thieno[2,3-b]-benzothiopyran structures

Research output: Contribution to journalArticlepeer-review

Abstract

Dihydrothieno[2,3-b]-benzothiopyran-4-ones are easily obtained by an intermolecular radical addition to an unactivated olefin using an S-o- fluorophenacyl xanthate followed by a novel, base induced domino cyclisation.

Original languageEnglish
Pages (from-to)2529-2532
Number of pages4
JournalTetrahedron Letters
Volume40
Issue number13
DOIs
Publication statusPublished - 26 Mar 1999

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