Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles
V A Mamedov
1, 2
,
A I Zamaletdinova
1, 2
,
V V Syakaev
1
,
E A Khafizova
1
,
Sh K Latypov
1
,
O G Sinyashin
1, 2
Publication type: Journal Article
Publication date: 2019-05-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
1-(Cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine react with ethyl bromopyruvate in refluxing dioxane to afford the corresponding 4,5,6,7-tetrahydroindole derivatives. Possibility to convert the synthesized compounds into their aromatic counterparts was exemplified by one model compound.
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Citations from 2024:
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Mamedov V. A. et al. Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles // Russian Chemical Bulletin. 2019. Vol. 68. No. 5. pp. 1014-1019.
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Mamedov V. A., Zamaletdinova A. I., Syakaev V. V., Khafizova E. A., Latypov S. K., Sinyashin O. G. Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles // Russian Chemical Bulletin. 2019. Vol. 68. No. 5. pp. 1014-1019.
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TY - JOUR
DO - 10.1007/s11172-019-2512-5
UR - https://doi.org/10.1007/s11172-019-2512-5
TI - Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles
T2 - Russian Chemical Bulletin
AU - Mamedov, V A
AU - Zamaletdinova, A I
AU - Syakaev, V V
AU - Khafizova, E A
AU - Latypov, Sh K
AU - Sinyashin, O G
PY - 2019
DA - 2019/05/01
PB - Springer Nature
SP - 1014-1019
IS - 5
VL - 68
SN - 1066-5285
SN - 1573-9171
ER -
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BibTex (up to 50 authors)
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@article{2019_Mamedov,
author = {V A Mamedov and A I Zamaletdinova and V V Syakaev and E A Khafizova and Sh K Latypov and O G Sinyashin},
title = {Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles},
journal = {Russian Chemical Bulletin},
year = {2019},
volume = {68},
publisher = {Springer Nature},
month = {may},
url = {https://doi.org/10.1007/s11172-019-2512-5},
number = {5},
pages = {1014--1019},
doi = {10.1007/s11172-019-2512-5}
}
Cite this
MLA
Copy
Mamedov, V. A., et al. “Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles.” Russian Chemical Bulletin, vol. 68, no. 5, May. 2019, pp. 1014-1019. https://doi.org/10.1007/s11172-019-2512-5.
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