Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid.
Publication type: Journal Article
Publication date: 2012-09-20
scimago Q2
wos Q1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
PubMed ID:
22994557
Organic Chemistry
Abstract
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the two-step, one-pot borylation/Suzuki cross-coupling reaction between aryl and heteroaryl halides. With use of Buchwald's second-generation XPhos preformed catalyst, high yields of cross-coupled products were obtained for most substrates. The method also allows an efficient two-step, one-pot synthesis, providing access to three distinct cross-coupled products after column chromatography. The method also provides a rapid and convenient route to teraryl compounds.
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117
Total citations:
117
Citations from 2024:
13
(11.2%)
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GOST
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Molander G. A., Trice S. L. J., Kennedy S. M. Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid. // Journal of Organic Chemistry. 2012. Vol. 77. No. 19. pp. 8678-8688.
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Molander G. A., Trice S. L. J., Kennedy S. M. Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid. // Journal of Organic Chemistry. 2012. Vol. 77. No. 19. pp. 8678-8688.
Cite this
RIS
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TY - JOUR
DO - 10.1021/jo301642v
UR - https://doi.org/10.1021/jo301642v
TI - Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid.
T2 - Journal of Organic Chemistry
AU - Molander, Gary A.
AU - Trice, Sarah L J
AU - Kennedy, Steven M
PY - 2012
DA - 2012/09/20
PB - American Chemical Society (ACS)
SP - 8678-8688
IS - 19
VL - 77
PMID - 22994557
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2012_Molander,
author = {Gary A. Molander and Sarah L J Trice and Steven M Kennedy},
title = {Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid.},
journal = {Journal of Organic Chemistry},
year = {2012},
volume = {77},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/jo301642v},
number = {19},
pages = {8678--8688},
doi = {10.1021/jo301642v}
}
Cite this
MLA
Copy
Molander, Gary A., et al. “Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid..” Journal of Organic Chemistry, vol. 77, no. 19, Sep. 2012, pp. 8678-8688. https://doi.org/10.1021/jo301642v.