Light-Mediated Sulfur–Boron Exchange
Publication type: Journal Article
Publication date: 2021-04-30
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
33929210
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Interaction of sulfides bearing a tetrafluoropyridinyl group with bis(catecholato)diboron followed by treatment with pinacol and triethylamine affording pinacol boronic esters is described. The reaction is promoted by an organic photocatalyst (3DPA2FBN) under irradiation with 400 nm light, and works with primary, secondary, and tertiary sulfides. The electron depleting character of the fluorinated pyridine fragment plays an important role in generating alkyl radicals.
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Total citations:
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Citations from 2024:
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(20%)
Cite this
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MLA
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GOST
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Panferova L. I., Dilman A. D. Light-Mediated Sulfur–Boron Exchange // Organic Letters. 2021. Vol. 23. No. 10. pp. 3919-3922.
GOST all authors (up to 50)
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Panferova L. I., Dilman A. D. Light-Mediated Sulfur–Boron Exchange // Organic Letters. 2021. Vol. 23. No. 10. pp. 3919-3922.
Cite this
RIS
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TY - JOUR
DO - 10.1021/acs.orglett.1c01080
UR - https://doi.org/10.1021/acs.orglett.1c01080
TI - Light-Mediated Sulfur–Boron Exchange
T2 - Organic Letters
AU - Panferova, Liubov I
AU - Dilman, Alexander D
PY - 2021
DA - 2021/04/30
PB - American Chemical Society (ACS)
SP - 3919-3922
IS - 10
VL - 23
PMID - 33929210
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2021_Panferova,
author = {Liubov I Panferova and Alexander D Dilman},
title = {Light-Mediated Sulfur–Boron Exchange},
journal = {Organic Letters},
year = {2021},
volume = {23},
publisher = {American Chemical Society (ACS)},
month = {apr},
url = {https://doi.org/10.1021/acs.orglett.1c01080},
number = {10},
pages = {3919--3922},
doi = {10.1021/acs.orglett.1c01080}
}
Cite this
MLA
Copy
Panferova, Liubov I., and Alexander D Dilman. “Light-Mediated Sulfur–Boron Exchange.” Organic Letters, vol. 23, no. 10, Apr. 2021, pp. 3919-3922. https://doi.org/10.1021/acs.orglett.1c01080.
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