Rhodium(NHC)-catalyzed amination of aryl bromides.Org Lett. 2010 Apr 02; 12(7):1640-3.OL
Abstract
A rhodium-catalyzed amination reaction of aryl halides with amines has been developed with the use of a N-heterocyclic carbene (NHC) ligand (IiPr = 1,3-diisopropylimidazol-2-ylidene). The active metal species responsible for the reaction progress was identified. The developed procedure of the Rh-catalyzedN-arylation is convenient to carry out under mild reaction conditions displaying a wide range of substrate scope and high degree of functional group tolerance.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
20205466
Citation
Kim, Min, and Sukbok Chang. "Rhodium(NHC)-catalyzed Amination of Aryl Bromides." Organic Letters, vol. 12, no. 7, 2010, pp. 1640-3.
Kim M, Chang S. Rhodium(NHC)-catalyzed amination of aryl bromides. Org Lett. 2010;12(7):1640-3.
Kim, M., & Chang, S. (2010). Rhodium(NHC)-catalyzed amination of aryl bromides. Organic Letters, 12(7), 1640-3. https://doi.org/10.1021/ol100437j
Kim M, Chang S. Rhodium(NHC)-catalyzed Amination of Aryl Bromides. Org Lett. 2010 Apr 2;12(7):1640-3. PubMed PMID: 20205466.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Rhodium(NHC)-catalyzed amination of aryl bromides.
AU - Kim,Min,
AU - Chang,Sukbok,
PY - 2010/3/9/entrez
PY - 2010/3/9/pubmed
PY - 2010/6/25/medline
SP - 1640
EP - 3
JF - Organic letters
JO - Org Lett
VL - 12
IS - 7
N2 - A rhodium-catalyzed amination reaction of aryl halides with amines has been developed with the use of a N-heterocyclic carbene (NHC) ligand (IiPr = 1,3-diisopropylimidazol-2-ylidene). The active metal species responsible for the reaction progress was identified. The developed procedure of the Rh-catalyzedN-arylation is convenient to carry out under mild reaction conditions displaying a wide range of substrate scope and high degree of functional group tolerance.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/20205466/Rhodium_NHC__catalyzed_amination_of_aryl_bromides_
L2 - https://doi.org/10.1021/ol100437j
DB - PRIME
DP - Unbound Medicine
ER -