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  Studies toward Providencin: The Furanyl-Cyclobutanol Segment

Spohr, S. M., & Fürstner, A. (2023). Studies toward Providencin: The Furanyl-Cyclobutanol Segment. Organic Letters, 25(9), 1536-1540. doi:10.1021/acs.orglett.3c00327.

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ol3c00327_si_001.pdf (Supplementary material), 9MB
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 Creators:
Spohr, Simon M.1, Author           
Fürstner, Alois1, Author           
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1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: The furanocembranoid providencin remains an unconquered bastion, although the synthesis of 17-deoxyprovidencin─lacking a single −OH group─has been accomplished in the past. This paper describes a practical approach to a properly hydroxylated building block via an iridium-catalyzed photosensitized intramolecular [2 + 2] cycloaddition as the key step. While an attempt to convert this compound into providencin via RCAM failed, it might well be elaborated into the natural product by adopting the literature route.

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Language(s): eng - English
 Dates: 2023-02-012023-02-272023-03-10
 Publication Status: Issued
 Pages: 5
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acs.orglett.3c00327
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Title: Organic Letters
  Abbreviation : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 25 (9) Sequence Number: - Start / End Page: 1536 - 1540 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338