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  Expedient Preparation of Trifluoromethyl-Substituted Benzofuranols

Morandi, B., & Carreira, E. M. (2011). Expedient Preparation of Trifluoromethyl-Substituted Benzofuranols. Organic Letters, 13(22), 5984-5985. doi:10.1021/ol202423s.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0026-A20E-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0026-A20F-2
Genre: Journal Article

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 Creators:
Morandi, Bill1, 2, Author           
Carreira, Erick M.2, Author
Affiliations:
1Research Group Morandi, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2040309              
2Laboratorium für Organische Chemie, ETH Zürich, CH-8093 Zürich, Switzerland, ou_persistent22              

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 Abstract: Direct access to 3-trifluoromethyl-substituted benzofuranols is presented. The products are obtained in good yields from commercially available salicylaldehydes by using in situ generated trifluoromethyl diazomethane and boron trifluoride as an activator. As shown in a representative example, the products can be transformed into the corresponding trifluoromethyl-substituted benzofurans.

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Language(s): eng - English
 Dates: 2011-10-202011-11-18
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol202423s
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Title: Organic Letters
  Other : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 13 (22) Sequence Number: - Start / End Page: 5984 - 5985 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338