Efficient Synthesis of the Pyoverdine Chromophore: Expanding the Toolbox for the Preparation of Pyoverdine Conjugates

Abstract The pyoverdine chromophore is an important component of a family of siderophores which are secreted by the human pathogen Pseudomonas aeruginosa for iron absorption. In this study, an efficient and improved synthetic route to the chromophore structure is reported, beginning from readily available starting materials, D‐glutamic acid and L–DOPA. This strategy has not only delivered the first synthesis of the free pyoverdine D chromophore, but also offers potential access to a wide range of other pyoverdine chromophore species.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-09-20
DOI
https://doi.org/10.1002/ejoc.202400745
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Efficient Synthesis of the Pyoverdine Chromophore: Expanding the Toolbox for the Preparation of Pyoverdine Conjugates

Ian M. Eggleston, Albert Bolhuis, Tianzhu Zhang
1 citations
European Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
0.25
article

Efficient Synthesis of the Pyoverdine Chromophore: Expanding the Toolbox for the Preparation of Pyoverdine Conjugates

Ian M. Eggleston, Albert Bolhuis, Tianzhu Zhang
article en
1 citations

Abstract

Abstract The pyoverdine chromophore is an important component of a family of siderophores which are secreted by the human pathogen Pseudomonas aeruginosa for iron absorption. In this study, an efficient and improved synthetic route to the chromophore structure is reported, beginning from readily available starting materials, D‐glutamic acid and L–DOPA. This strategy has not only delivered the first synthesis of the free pyoverdine D chromophore, but also offers potential access to a wide range of other pyoverdine chromophore species.

European Journal of Organic ChemistryVol. 27(46)
University of Bath (GB)
University of Bath
Openalex Percentile: Top 48%
Oxidative Organic Chemistry Reactions
0.25
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