Synthesis of 5-Halo-4H-1,3-oxazine-6-amines by a copper-mediated domino reaction

Three become one! In one copper-mediated step, three simple components, including a propargylcarboxamide, a protected amine, and a source of chloride, assemble to give highly functionalized oxazines, which are interesting building blocks for the synthesis of other aminooxazine derivatives (see schem...

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Bibliographic Details
Main Authors: Hashmi, A. Stephen K. (Author) , Schuster, Andreas M. (Author) , Zimmer, Marc (Author) , Rominger, Frank (Author)
Format: Article (Journal)
Language:English
Published: 13 April 2011
In: Chemistry - a European journal
Year: 2011, Volume: 17, Issue: 20, Pages: 5511-5515
ISSN:1521-3765
DOI:10.1002/chem.201100423
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/chem.201100423
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201100423
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Author Notes:A. Stephen K. Hashmi, Andreas M. Schuster, Marc Zimmer, and Frank Rominger
Description
Summary:Three become one! In one copper-mediated step, three simple components, including a propargylcarboxamide, a protected amine, and a source of chloride, assemble to give highly functionalized oxazines, which are interesting building blocks for the synthesis of other aminooxazine derivatives (see scheme; R1=range of aryl or alkyl groups, R2=alkyl, EWG=electron-withdrawing group).
Item Description:Gesehen am 07.09.2022
Physical Description:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201100423