Diversity-oriented derivatization of BODIPY based on regioselective bromination
Publication type: Journal Article
Publication date: 2012-01-26
scimago Q2
wos Q2
SJR: 0.600
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
22334235
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Regioselectively brominated BODIPYs were shown to undergo nucleophilic substitution and Sonogashira coupling reactions with a one-pot procedure, yielding diversely substituted fluorophores.
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17
Total citations:
17
Citations from 2024:
2
(11.76%)
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GOST
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Li X., Huang S., Hu Y. Diversity-oriented derivatization of BODIPY based on regioselective bromination // Organic and Biomolecular Chemistry. 2012. Vol. 10. No. 12. p. 2369.
GOST all authors (up to 50)
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Li X., Huang S., Hu Y. Diversity-oriented derivatization of BODIPY based on regioselective bromination // Organic and Biomolecular Chemistry. 2012. Vol. 10. No. 12. p. 2369.
Cite this
RIS
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TY - JOUR
DO - 10.1039/c2ob07004a
UR - https://doi.org/10.1039/c2ob07004a
TI - Diversity-oriented derivatization of BODIPY based on regioselective bromination
T2 - Organic and Biomolecular Chemistry
AU - Li, Xiaolin
AU - Huang, Shufang
AU - Hu, Yongzhou
PY - 2012
DA - 2012/01/26
PB - Royal Society of Chemistry (RSC)
SP - 2369
IS - 12
VL - 10
PMID - 22334235
SN - 1477-0520
SN - 1477-0539
ER -
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BibTex (up to 50 authors)
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@article{2012_Li,
author = {Xiaolin Li and Shufang Huang and Yongzhou Hu},
title = {Diversity-oriented derivatization of BODIPY based on regioselective bromination},
journal = {Organic and Biomolecular Chemistry},
year = {2012},
volume = {10},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c2ob07004a},
number = {12},
pages = {2369},
doi = {10.1039/c2ob07004a}
}
Cite this
MLA
Copy
Li, Xiaolin, et al. “Diversity-oriented derivatization of BODIPY based on regioselective bromination.” Organic and Biomolecular Chemistry, vol. 10, no. 12, Jan. 2012, p. 2369. https://doi.org/10.1039/c2ob07004a.