Aerobic Ru-catalyzed direct C2-olefination of N-heteroarenes with alkenes directed by a removable N-dimethylcarbamoyl group.Chem Commun (Camb). 2013 Oct 09; 49(78):8830-2.CC
Abstract
A highly efficient and selective Ru-catalyzed direct C2-olefination of indoles, pyrroles, and carbazoles assisted by a removable N-dimethylcarbamoyl group has been developed by using O2 as the terminal oxidant. Both electron-deficient and unactivated alkenes are applicable to the protocol.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
23959021
Citation
Zhang, Luo-Qiang, et al. "Aerobic Ru-catalyzed Direct C2-olefination of N-heteroarenes With Alkenes Directed By a Removable N-dimethylcarbamoyl Group." Chemical Communications (Cambridge, England), vol. 49, no. 78, 2013, pp. 8830-2.
Zhang LQ, Yang S, Huang X, et al. Aerobic Ru-catalyzed direct C2-olefination of N-heteroarenes with alkenes directed by a removable N-dimethylcarbamoyl group. Chem Commun (Camb). 2013;49(78):8830-2.
Zhang, L. Q., Yang, S., Huang, X., You, J., & Song, F. (2013). Aerobic Ru-catalyzed direct C2-olefination of N-heteroarenes with alkenes directed by a removable N-dimethylcarbamoyl group. Chemical Communications (Cambridge, England), 49(78), 8830-2. https://doi.org/10.1039/c3cc44787a
Zhang LQ, et al. Aerobic Ru-catalyzed Direct C2-olefination of N-heteroarenes With Alkenes Directed By a Removable N-dimethylcarbamoyl Group. Chem Commun (Camb). 2013 Oct 9;49(78):8830-2. PubMed PMID: 23959021.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Aerobic Ru-catalyzed direct C2-olefination of N-heteroarenes with alkenes directed by a removable N-dimethylcarbamoyl group.
AU - Zhang,Luo-Qiang,
AU - Yang,Shiping,
AU - Huang,Xiaolei,
AU - You,Jingsong,
AU - Song,Feijie,
PY - 2013/8/21/entrez
PY - 2013/8/21/pubmed
PY - 2014/3/25/medline
SP - 8830
EP - 2
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
VL - 49
IS - 78
N2 - A highly efficient and selective Ru-catalyzed direct C2-olefination of indoles, pyrroles, and carbazoles assisted by a removable N-dimethylcarbamoyl group has been developed by using O2 as the terminal oxidant. Both electron-deficient and unactivated alkenes are applicable to the protocol.
SN - 1364-548X
UR - https://www.unboundmedicine.com/medline/citation/23959021/Aerobic_Ru_catalyzed_direct_C2_olefination_of_N_heteroarenes_with_alkenes_directed_by_a_removable_N_dimethylcarbamoyl_group_
L2 - https://doi.org/10.1039/c3cc44787a
DB - PRIME
DP - Unbound Medicine
ER -