Hypervalent iodine(III)-induced domino oxidative cyclization for the synthesis of cyclopenta[b]furans

Mei Huey Lin, Yu Chun Chen, Shih Hao Chiu, Yun Fan Chen, Tsung Hsun Chuang

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

A new strategy for cyclopenta[b]furan synthesis mediated by hypervalent iodine(III) has been described. The approach employs diacetoxyiodobenzene-induced initial dehydrogenation to a putative trienone intermediate and triggered sequential cycloisomerization to form the cyclo-penta[b]furan targets.

Original languageEnglish
Article number1713
JournalMolecules
Volume21
Issue number12
DOIs
Publication statusPublished - 2016 Dec 1

Fingerprint

Furans
furans
Cyclization
Iodine
iodine
Rubiaceae
Dehydrogenation
synthesis
dehydrogenation
furan

All Science Journal Classification (ASJC) codes

  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Pharmaceutical Science
  • Drug Discovery
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Lin, Mei Huey ; Chen, Yu Chun ; Chiu, Shih Hao ; Chen, Yun Fan ; Chuang, Tsung Hsun. / Hypervalent iodine(III)-induced domino oxidative cyclization for the synthesis of cyclopenta[b]furans. In: Molecules. 2016 ; Vol. 21, No. 12.
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Hypervalent iodine(III)-induced domino oxidative cyclization for the synthesis of cyclopenta[b]furans. / Lin, Mei Huey; Chen, Yu Chun; Chiu, Shih Hao; Chen, Yun Fan; Chuang, Tsung Hsun.

In: Molecules, Vol. 21, No. 12, 1713, 01.12.2016.

Research output: Contribution to journalArticle

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AU - Chuang, Tsung Hsun

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