Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles
Publication type: Journal Article
Publication date: 2012-11-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
1,4-Nucleophilic addition reactions of 3-nitrothiochromone with indoles gave a number of novel trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones in 36–89% yields. During the reactions, the thiopyrone ring underwent no opening.
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Barabanov M. A., Sevenard D., Sosnovskikh V. Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles // Russian Chemical Bulletin. 2012. Vol. 61. No. 11. pp. 2183-2185.
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Barabanov M. A., Sevenard D., Sosnovskikh V. Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles // Russian Chemical Bulletin. 2012. Vol. 61. No. 11. pp. 2183-2185.
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TY - JOUR
DO - 10.1007/s11172-012-0308-y
UR - https://doi.org/10.1007/s11172-012-0308-y
TI - Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles
T2 - Russian Chemical Bulletin
AU - Barabanov, M A
AU - Sevenard, D.V
AU - Sosnovskikh, V.Ya
PY - 2012
DA - 2012/11/01
PB - Springer Nature
SP - 2183-2185
IS - 11
VL - 61
SN - 1066-5285
SN - 1573-9171
ER -
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BibTex (up to 50 authors)
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@article{2012_Barabanov,
author = {M A Barabanov and D.V Sevenard and V.Ya Sosnovskikh},
title = {Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles},
journal = {Russian Chemical Bulletin},
year = {2012},
volume = {61},
publisher = {Springer Nature},
month = {nov},
url = {https://doi.org/10.1007/s11172-012-0308-y},
number = {11},
pages = {2183--2185},
doi = {10.1007/s11172-012-0308-y}
}
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MLA
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Barabanov, M. A., et al. “Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles.” Russian Chemical Bulletin, vol. 61, no. 11, Nov. 2012, pp. 2183-2185. https://doi.org/10.1007/s11172-012-0308-y.
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