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  Base-Promoted Internal Redox-Cyclisation Reactions

Shaaban, S., Peng, B., & Maulide, N. (2013). Base-Promoted Internal Redox-Cyclisation Reactions. Synlett, 24(13), 1722-1724. doi:10.1055/s-0033-1339313.

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 Creators:
Shaaban, Saad1, Author           
Peng, Bo1, Author           
Maulide, Nuno1, Author           
Affiliations:
1Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445614              

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Free keywords: C-H activation - C-H functionalisation - redox - cyclisation - pyrrolidine
 Abstract: A new internal, base-mediated redox-cyclisation reaction has been discovered and developed. In this transformation, the sacrificial reduction of an alkynyl moiety to an alkene allows direct functionalisation of an α-amino C-H bond. This approach allows the preparation of several 1,3-oxazinane derivatives in an atom-­efficient manner.

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Language(s): eng - English
 Dates: 2013-07-10
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1055/s-0033-1339313
 Degree: -

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Title: Synlett
  Other : Synlett
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 24 (13) Sequence Number: - Start / End Page: 1722 - 1724 Identifier: ISSN: 0936-5214
CoNE: https://pure.mpg.de/cone/journals/resource/954925570856