The Chan–Evans–Lam N-Arylation of 2-Imidazolines
Publication type: Journal Article
Publication date: 2016-11-30
scimago Q2
wos Q1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
PubMed ID:
27978721
Organic Chemistry
Abstract
N-Arylation of 2-imidazolines with arylboronic acids promoted by copper(II) acetate in DMSO provides an attractive alternative to the earlier reported transition metal-catalyzed approaches employing (hetero)aryl halides as it taps into the vast reagent space of commercially available boronic acids and proceeds at ambient temperature. Many of the resulting compounds are distinctly lead-like, thus positioning the method developed well within the toolbox of lead-oriented synthesis.
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Metrics
24
Total citations:
24
Citations from 2024:
1
(4.17%)
Cite this
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BibTex |
MLA
Cite this
GOST
Copy
Dar’in D., Krasavin M. The Chan–Evans–Lam N-Arylation of 2-Imidazolines // Journal of Organic Chemistry. 2016. Vol. 81. No. 24. pp. 12514-12519.
GOST all authors (up to 50)
Copy
Dar’in D., Krasavin M. The Chan–Evans–Lam N-Arylation of 2-Imidazolines // Journal of Organic Chemistry. 2016. Vol. 81. No. 24. pp. 12514-12519.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/acs.joc.6b02404
UR - https://doi.org/10.1021/acs.joc.6b02404
TI - The Chan–Evans–Lam N-Arylation of 2-Imidazolines
T2 - Journal of Organic Chemistry
AU - Dar’in, Dmitry
AU - Krasavin, Mikhail
PY - 2016
DA - 2016/11/30
PB - American Chemical Society (ACS)
SP - 12514-12519
IS - 24
VL - 81
PMID - 27978721
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2016_Dar’in,
author = {Dmitry Dar’in and Mikhail Krasavin},
title = {The Chan–Evans–Lam N-Arylation of 2-Imidazolines},
journal = {Journal of Organic Chemistry},
year = {2016},
volume = {81},
publisher = {American Chemical Society (ACS)},
month = {nov},
url = {https://doi.org/10.1021/acs.joc.6b02404},
number = {24},
pages = {12514--12519},
doi = {10.1021/acs.joc.6b02404}
}
Cite this
MLA
Copy
Dar’in, Dmitry, and Mikhail Krasavin. “The Chan–Evans–Lam N-Arylation of 2-Imidazolines.” Journal of Organic Chemistry, vol. 81, no. 24, Nov. 2016, pp. 12514-12519. https://doi.org/10.1021/acs.joc.6b02404.
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