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  Stereoselective Synthesis of Enamides by a Peterson Reaction Manifold

Fürstner, A., Brehm, C., & Cancho-Grande, Y. (2001). Stereoselective Synthesis of Enamides by a Peterson Reaction Manifold. Organic Letters, 3(24), 3955-3957. doi:10.1021/ol016848p.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-45EC-D Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-45ED-B
Genre: Journal Article

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 Creators:
Fürstner, Alois1, Author           
Brehm, Christof1, Author           
Cancho-Grande, Yolande1, Author
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1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: Vinylsilanes are converted into enamides by a sequence comprising epoxidation, nucleophilic ring opening of the resulting epoxysilanes with NaN3, and reduction of the azide, followed by a “one-pot” N-acylation/Peterson elimination process. This method is distinguished by its wide applicability and stereoselective course.

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Language(s): eng - English
 Dates: 2001-10-032001-11-082001-11-29
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol016848p
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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: 3 Volume / Issue: 3 (24) Sequence Number: - Start / End Page: 3955 - 3957 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338