Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility
Clara Uriel
1
,
Ana M Gómez
1
,
Enrique García Martínez De La Hidalga
2
,
Jorge Bañuelos
2
,
Inmaculada García-Moreno
3
,
J.Cristóbal López
1
Publication type: Journal Article
Publication date: 2021-08-17
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
34403255
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Hitherto unreported 2,6-dipropargyl-1,3,5,7-tetramethyl BODIPYs can be efficiently prepared by a Nicholas reaction/decomplexation protocol from 1,3,5,7-tetramethyl BODIPYs. The title compounds, which improve the BODIPY photostability by retaining their inherent photophysical and photochemical properties, can be engaged in efficient copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) "click-type" reactions with azido derivatives to provide all-BODIPY-triads or conjugated BODIPYs.
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Total citations:
20
Citations from 2024:
9
(45%)
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GOST
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Uriel C. et al. Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility // Organic Letters. 2021. Vol. 23. No. 17. pp. 6801-6806.
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Uriel C., Gómez A. M., García Martínez De La Hidalga E., Bañuelos J., García-Moreno I., López J. Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility // Organic Letters. 2021. Vol. 23. No. 17. pp. 6801-6806.
Cite this
RIS
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TY - JOUR
DO - 10.1021/acs.orglett.1c02380
UR - https://doi.org/10.1021/acs.orglett.1c02380
TI - Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility
T2 - Organic Letters
AU - Uriel, Clara
AU - Gómez, Ana M
AU - García Martínez De La Hidalga, Enrique
AU - Bañuelos, Jorge
AU - García-Moreno, Inmaculada
AU - López, J.Cristóbal
PY - 2021
DA - 2021/08/17
PB - American Chemical Society (ACS)
SP - 6801-6806
IS - 17
VL - 23
PMID - 34403255
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2021_Uriel,
author = {Clara Uriel and Ana M Gómez and Enrique García Martínez De La Hidalga and Jorge Bañuelos and Inmaculada García-Moreno and J.Cristóbal López},
title = {Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility},
journal = {Organic Letters},
year = {2021},
volume = {23},
publisher = {American Chemical Society (ACS)},
month = {aug},
url = {https://doi.org/10.1021/acs.orglett.1c02380},
number = {17},
pages = {6801--6806},
doi = {10.1021/acs.orglett.1c02380}
}
Cite this
MLA
Copy
Uriel, Clara, et al. “Access to 2,6-Dipropargylated BODIPYs as “Clickable” Congeners of Pyrromethene-567 Dye: Photostability and Synthetic Versatility.” Organic Letters, vol. 23, no. 17, Aug. 2021, pp. 6801-6806. https://doi.org/10.1021/acs.orglett.1c02380.