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Journal articles
Application of the Curtius rearrangement to the synthesis of 1′-aminoferrocene-1-carboxylic acid derivatives
Abstract : The shortest synthesis of N-protected 1′-aminoferrocene-1-carboxylic acid from readily available ferrocene-1,1′-dicarboxylic acid is reported. 1′-Azidocarbonylferrocene-1-carboxylic acid was first obtained by reaction of the latter with diphenylphosphoryl azide. It was then converted into four amino acids by a Curtius rearrangement conducted in the presence of tert-butanol, benzyl alcohol, 9-fluorenemethanol or allyl alcohol. The benzyl and allyl carbamate derivatives are reported and characterized for the first time. The four corresponding new succinimidyl activated esters were also prepared and their usefulness was demonstrated in peptide coupling. Various structures were elucidated by X-ray crystallography, including 1′-azidocarbonylferrocene-1-carboxylic acid and 1,1′-diazidocarbonylferrocene. © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
Cited literature [43 references]
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01740157
Contributor : Laurent Jonchère Connect in order to contact the contributor
Submitted on : Thursday, April 26, 2018 - 12:12:19 PM
Last modification on : Wednesday, April 7, 2021 - 3:18:09 PM
Long-term archiving on: : Thursday, September 20, 2018 - 4:56:52 AM
Contributor : Laurent Jonchère Connect in order to contact the contributor
Submitted on : Thursday, April 26, 2018 - 12:12:19 PM
Last modification on : Wednesday, April 7, 2021 - 3:18:09 PM
Long-term archiving on: : Thursday, September 20, 2018 - 4:56:52 AM