volume 47 issue 4 pages 425-434

Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system

I V Taydakov 1
T Ya Dutova 2
E N Sidorenko 2
S S Krasnoselsky 3
1
 
G. S. Petrov Institute of Plastics, Moscow, Russia
2
 
State Research Center for Antibiotics, Moscow, Russia
Publication typeJournal Article
Publication date2011-07-01
scimago Q4
wos Q4
SJR0.243
CiteScore2.7
Impact factor1.0
ISSN00093122, 15738353
Organic Chemistry
Abstract
A new catalytic system containing ferric chloride, activated carbon, and hydrazine has been proposed for the reductive cyclization of β-dialkylamino-2-nitrostyrenes to give the corresponding indoles (Leimgruber-Batcho synthesis). Various substituted indoles may be obtained in high yield under these conditions.
Found 
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Taydakov I. V. et al. Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system // Chemistry of Heterocyclic Compounds. 2011. Vol. 47. No. 4. pp. 425-434.
GOST all authors (up to 50) Copy
Taydakov I. V., Dutova T. Ya., Sidorenko E. N., Krasnoselsky S. S. Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system // Chemistry of Heterocyclic Compounds. 2011. Vol. 47. No. 4. pp. 425-434.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1007/s10593-011-0776-2
UR - https://doi.org/10.1007/s10593-011-0776-2
TI - Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system
T2 - Chemistry of Heterocyclic Compounds
AU - Taydakov, I V
AU - Dutova, T Ya
AU - Sidorenko, E N
AU - Krasnoselsky, S S
PY - 2011
DA - 2011/07/01
PB - Springer Nature
SP - 425-434
IS - 4
VL - 47
SN - 0009-3122
SN - 1573-8353
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2011_Taydakov,
author = {I V Taydakov and T Ya Dutova and E N Sidorenko and S S Krasnoselsky},
title = {Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system},
journal = {Chemistry of Heterocyclic Compounds},
year = {2011},
volume = {47},
publisher = {Springer Nature},
month = {jul},
url = {https://doi.org/10.1007/s10593-011-0776-2},
number = {4},
pages = {425--434},
doi = {10.1007/s10593-011-0776-2}
}
MLA
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MLA Copy
Taydakov, I. V., et al. “Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system.” Chemistry of Heterocyclic Compounds, vol. 47, no. 4, Jul. 2011, pp. 425-434. https://doi.org/10.1007/s10593-011-0776-2.