Published in
Royal Society of Chemistry, Organic Chemistry Frontiers, 2024
DOI: 10.1039/d4qo00886c
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Chemoselective reaction of methoxyaminomethyl BODIPYs with unprotected carbohydrates: a powerful tool for accessing BODIPY neoglycosides
Journal article published in 2024 by
Ana M. Gómez 
,
Luis García-Fernández ,
Andrés G. Santana ,
Clara Uriel,
Leire Gartzia-Rivero ,
Jorge Bañuelos ,
Inmaculada Garcia-Moreno,
Lourdes Infantes ,
María Rosa Aguilar ,
J. Cristobal Lopez
,
Luis García-Fernández ,
Andrés G. Santana ,
Clara Uriel,
Leire Gartzia-Rivero ,
Jorge Bañuelos ,
Inmaculada Garcia-Moreno,
Lourdes Infantes ,
María Rosa Aguilar ,
J. Cristobal Lopez
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Abstract
The neoglycosylation of methoxyaminomethyl BODIPYs with unprotected reducing saccharides produces cyclic N-glycosyl-N-methoxy-BODIPY conjugates, which display excellent photophysical characteristics in pure water, even at high dye concentrations.