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

doi:10.3390/molecules21121713

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

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

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 language	English
Article number	1713
Journal	Molecules
Volume	21
Issue number	12
DOIs	https://doi.org/10.3390/molecules21121713
Publication status	Published - 2016 Dec 1

All Science Journal Classification (ASJC) codes

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

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10.3390/molecules21121713

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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.",

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AU - Chuang, Tsung Hsun

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