Acid-Catalyzed Skeletal Reorganization of Phenyloxirane Derivatives
-alkynylphenyl oxiranes underwent skeletal rearrangement under Brønsted and Lewis acid conditions to give indenylfuran and indanylbenzofuran frameworks, respectively. The transformations proceeded under mild conditions with broad substrate tolerance and were generally insensitive to electronic effects.
Authors
- Bundet Boekfa (ORCID: https://orcid.org/0000-0002-9281-9405)
- Chayamon Chantana
- Jumreang Tummatorn (ORCID: https://orcid.org/0000-0002-1662-151X)
- Chatphorn Theppitak (ORCID: https://orcid.org/0000-0003-2091-4937)
- Charnsak Thongsornkleeb (ORCID: https://orcid.org/0000-0003-2653-5137)
- Somsak Ruchirawat
Institutions
- Kasetsart University (TH)
- Chulabhorn Graduate Institute (TH)
- Chulabhorn Research Institute (TH)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-05-08
- DOI
- https://doi.org/10.1021/acs.orglett.6c01474
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Thailand Science Research and Innovation
- Chulabhorn Graduate Institute, Chulabhorn Royal Academy