A straightforward synthesis of benzothiazines

Carolina Gimbert, Adelina Vallribera

Research output: Contribution to journalArticleResearchpeer-review

29 Citations (Scopus)

Abstract

(Chemical Equation Presented) A series of 4H-3,1-benzothiazines have been successfully synthesized through a three-step sequence starting from commercially available 2-iodoaniline. The key step consists of the cyclization of compounds 6 via an intramolecular S-conjugate addition. The synthesis is straightforward, gives good yields and offers a broad range of possibilities since R can be many alkyl or aryl groups and Z a suitable electron-withdrawing functionalization. © 2009 American Chemical Society.
Original languageEnglish
Pages (from-to)269-271
JournalOrganic Letters
Volume11
Issue number2
DOIs
Publication statusPublished - 15 Jan 2009

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