Premium
Convenient Access to Carbohydrate–BODIPY Hybrids by Two Complementary Methods Involving One‐Pot Assembly of “Clickable” BODIPY Dyes (Eur. J. Org. Chem. 26/2014)
Author(s) -
MartinezGonzalez Mayra R.,
UríasBenavides Arlette,
AlvaradoMartínez Enrique,
Lopez J. Cristobal,
Gómez Ana M.,
del Rio Mayca,
Garcia Inmaculada,
Costela Angel,
Bañuelos Jorge,
Arbeloa Teresa,
Lopez Arbeloa Iñigo,
PeñaCabrera Eduardo
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201490072
Subject(s) - bodipy , chemistry , carbohydrate , fluorescence , alkyne , combinatorial chemistry , boronic acid , ring (chemistry) , stereochemistry , organic chemistry , physics , quantum mechanics , catalysis
The cover picture shows two concise, complementary, protocols for the one‐pot, three‐component assembly of an alkyne‐ or azido‐carbohydrate, 8‐thiomethyl BODIPY, and either propargylamine or an azido boronic acid, respectively, which allow access to fluorescent carbohydrate–BODIPY hybrids. These carbohydrate–BODIPY hybrids display excellent photophysical and laser properties that relate to the spacer employed (amino group or aromatic ring). Details are discussed in the Short Communication by J. C. Lopez, J. Bañuelos, E. Peña‐Cabrera et al. on p. 5659 ff .