volume 51 issue 33 pages 7136-7139

Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity

Publication typeJournal Article
Publication date2015-03-16
scimago Q1
wos Q2
SJR1.037
CiteScore7.4
Impact factor4.2
ISSN13597345, 1364548X
PubMed ID:  25806709
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Abstract

The Mn-catalyzed C–H alkenylations of indole with terminal- and/or internal-alkynes have been developed to selectively yield indolylalkene and carbazole.

Found 
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GOST Copy
Shi L. et al. Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity // Chemical Communications. 2015. Vol. 51. No. 33. pp. 7136-7139.
GOST all authors (up to 50) Copy
Shi L., Zhong X., She H., Lei Z., Li F. Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity // Chemical Communications. 2015. Vol. 51. No. 33. pp. 7136-7139.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1039/c5cc00249d
UR - https://doi.org/10.1039/c5cc00249d
TI - Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
T2 - Chemical Communications
AU - Shi, Lijun
AU - Zhong, Xiang
AU - She, Houde
AU - Lei, Ziqiang
AU - Li, Fuwei
PY - 2015
DA - 2015/03/16
PB - Royal Society of Chemistry (RSC)
SP - 7136-7139
IS - 33
VL - 51
PMID - 25806709
SN - 1359-7345
SN - 1364-548X
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2015_Shi,
author = {Lijun Shi and Xiang Zhong and Houde She and Ziqiang Lei and Fuwei Li},
title = {Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity},
journal = {Chemical Communications},
year = {2015},
volume = {51},
publisher = {Royal Society of Chemistry (RSC)},
month = {mar},
url = {https://doi.org/10.1039/c5cc00249d},
number = {33},
pages = {7136--7139},
doi = {10.1039/c5cc00249d}
}
MLA
Cite this
MLA Copy
Shi, Lijun, et al. “Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity.” Chemical Communications, vol. 51, no. 33, Mar. 2015, pp. 7136-7139. https://doi.org/10.1039/c5cc00249d.