volume 78 issue 2 pages 757-761

Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs.

Publication typeJournal Article
Publication date2012-12-13
scimago Q2
wos Q1
SJR0.737
CiteScore6.1
Impact factor3.6
ISSN00223263, 15206904
PubMed ID:  23237433
Organic Chemistry
Abstract
A new method for the synthesis of Cl-BODIPYs from F-BODIPYs is reported, merely requiring treatment of the F-BODIPY with boron trichloride. Cl-BODIPYs are exploited as synthetic intermediates generated in situ for the overall conversion of F-BODIPYs to O- and C-BODIPYs in high overall yields using a mild one-pot procedure. This route enables F-BODIPYs to be transformed into derivatives that are not accessible via the direct route, as demonstrated via the use of 1,3-propanediol.
Found 
Found 

Top-30

Journals

1
2
3
4
5
Journal of Organic Chemistry
5 publications, 12.5%
Chemical Communications
4 publications, 10%
Inorganic Chemistry
3 publications, 7.5%
Organic and Biomolecular Chemistry
3 publications, 7.5%
Coordination Chemistry Reviews
2 publications, 5%
Advanced Functional Materials
2 publications, 5%
Beilstein Journal of Organic Chemistry
1 publication, 2.5%
Chinese Journal of Organic Chemistry
1 publication, 2.5%
Analytical Sciences
1 publication, 2.5%
Tetrahedron Letters
1 publication, 2.5%
Dyes and Pigments
1 publication, 2.5%
Sensors and Actuators, B: Chemical
1 publication, 2.5%
Chemistry - A European Journal
1 publication, 2.5%
European Journal of Organic Chemistry
1 publication, 2.5%
Journal of Physical Chemistry A
1 publication, 2.5%
ACS Omega
1 publication, 2.5%
Advanced Materials
1 publication, 2.5%
Chemical Society Reviews
1 publication, 2.5%
RSC Advances
1 publication, 2.5%
Journal of Materials Chemistry A
1 publication, 2.5%
Dalton Transactions
1 publication, 2.5%
Organic Chemistry Frontiers
1 publication, 2.5%
Advances in Heterocyclic Chemistry
1 publication, 2.5%
ChemMedChem
1 publication, 2.5%
Russian Chemical Reviews
1 publication, 2.5%
Molecules
1 publication, 2.5%
1
2
3
4
5

Publishers

2
4
6
8
10
12
Royal Society of Chemistry (RSC)
12 publications, 30%
American Chemical Society (ACS)
10 publications, 25%
Elsevier
6 publications, 15%
Wiley
6 publications, 15%
Beilstein-Institut
1 publication, 2.5%
Shanghai Institute of Organic Chemistry
1 publication, 2.5%
Japan Society for Analytical Chemistry
1 publication, 2.5%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.5%
MDPI
1 publication, 2.5%
2
4
6
8
10
12
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
40
Share
Cite this
GOST |
Cite this
GOST Copy
Lundrigan T., Thompson A. R. Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs. // Journal of Organic Chemistry. 2012. Vol. 78. No. 2. pp. 757-761.
GOST all authors (up to 50) Copy
Lundrigan T., Thompson A. R. Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs. // Journal of Organic Chemistry. 2012. Vol. 78. No. 2. pp. 757-761.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1021/jo302277d
UR - https://doi.org/10.1021/jo302277d
TI - Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs.
T2 - Journal of Organic Chemistry
AU - Lundrigan, Travis
AU - Thompson, Alison R
PY - 2012
DA - 2012/12/13
PB - American Chemical Society (ACS)
SP - 757-761
IS - 2
VL - 78
PMID - 23237433
SN - 0022-3263
SN - 1520-6904
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2012_Lundrigan,
author = {Travis Lundrigan and Alison R Thompson},
title = {Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs.},
journal = {Journal of Organic Chemistry},
year = {2012},
volume = {78},
publisher = {American Chemical Society (ACS)},
month = {dec},
url = {https://doi.org/10.1021/jo302277d},
number = {2},
pages = {757--761},
doi = {10.1021/jo302277d}
}
MLA
Cite this
MLA Copy
Lundrigan, Travis, and Alison R Thompson. “Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs..” Journal of Organic Chemistry, vol. 78, no. 2, Dec. 2012, pp. 757-761. https://doi.org/10.1021/jo302277d.