Chemoselective reaction of methoxyaminomethyl BODIPYs with unprotected carbohydrates: a powerful tool for accessing BODIPY neoglycosides-Reference-Cited by-同舟云学术

Chemoselective reaction of methoxyaminomethyl BODIPYs with unprotected carbohydrates: a powerful tool for accessing BODIPY neoglycosides

Published:2024 Issue:16 Volume:11 Page:4356-4365
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Gómez Ana M.¹^ORCID,García-Fernández Luis²³^ORCID,Santana Andrés G.¹^ORCID,Uriel Clara¹,Gartzia-Rivero Leire⁴^ORCID,Bañuelos Jorge⁴^ORCID,Garcia-Moreno Inmaculada⁵,Infantes Lourdes⁶^ORCID,Aguilar María Rosa²³^ORCID,Lopez J. Cristobal¹^ORCID

Affiliation:

1. Instituto de Química Orgánica General (IQOG-CSIC), Juan de la Cierva 3, 28006 Madrid, Spain

2. Instituto de Ciencia y Tecnología de Polímeros (ICTP-CSIC), Juan de la Cierva 3, 28006 Madrid, Spain

3. Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Instituto de Salud Carlos III, Monforte de Lemos 3-5, 28029 Madrid, Spain

4. Departamento de Química Física, Universidad del País Vasco (UPV/EHU), Apartado 644, 48080 Bilbao, Spain

5. Departamento de Química-Física de Materiales, Instituto de Química-Física “Blas Cabrera” (IQF-CSIC), Serrano 119, 28006 Madrid, Spain

6. Departamento de Cristalografía y Biología Estructural, Instituto de Química-Física “Blas Cabrera” (IQF-CSIC), Serrano 119, 28006 Madrid, Spain

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.

Funder

Comunidad de Madrid

Eusko Jaurlaritza

Ministerio de Ciencia e Innovación

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00886C

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