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Inside protonation of 1,8-diazabicyclo[6.6.n]alka-4,11-diynes

Protonation of 1,8-diazabicyclo[6.6.3]heptadeca-4,11-diyne (4a), 1,8-diazabicyclo[6.6.4]octa-deca-4,11-diyne (4b), 1,8-diazabicyclo[6.6.5]nonadeca-4,11-diyne (4c), and 1,8-diazabicyclo[6.6.6]eicosa-4,11-diyne (4d) was achieved by treatment of 4a−4d with strong acids. Monoprotonation products were is...

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Main Authors: Balalaie, Saeed (Author) , Kunze, Andreas (Author) , Gleiter, Rolf (Author) , Rominger, Frank (Author) , Geis, Sibylle (Author) , Oeser, Thomas (Author)
Format: Article (Journal)
Language:English
Published: 12 August 2003
In: European journal of organic chemistry
Year: 2003, Issue: 17, Pages: 3378-3381
ISSN:1099-0690
DOI:10.1002/ejoc.200300235
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejoc.200300235
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.200300235
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Author Notes:Saeed Balalaie, Andreas Kunze, Rolf Gleiter, Frank Rominger, Sibylle Geis, and Thomas Oeser

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