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Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones

Denis Sergeevich Baranov 1, 2
Denis Sergeevich Baranov
, 
Dmitry Sergeevich Fadeev 3
Dmitry Sergeevich Fadeev
10.1016/j.mencom.2016.03.032
Published 2016-03-02
Communication , Volume 26, Issue 2, 174-176
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Baranov D. S., Fadeev D. S. Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones // Mendeleev Communications. 2016. Vol. 26. No. 2. pp. 174-176.
GOST all authors (up to 50) Copy
Baranov D. S., Fadeev D. S. Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones // Mendeleev Communications. 2016. Vol. 26. No. 2. pp. 174-176.
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TY - JOUR
DO - 10.1016/j.mencom.2016.03.032
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.032
TI - Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones
T2 - Mendeleev Communications
AU - Baranov, Denis Sergeevich
AU - Fadeev, Dmitry Sergeevich
PY - 2016
DA - 2016/03/02
PB - Mendeleev Communications
SP - 174-176
IS - 2
VL - 26
ER -
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@article{2016_Baranov,
author = {Denis Sergeevich Baranov and Dmitry Sergeevich Fadeev},
title = {Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.032},
number = {2},
pages = {174--176},
doi = {10.1016/j.mencom.2016.03.032}
}
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Baranov, Denis Sergeevich, and Dmitry Sergeevich Fadeev. “Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones.” Mendeleev Communications, vol. 26, no. 2, Mar. 2016, pp. 174-176. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.032.

Abstract

New 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-benzylor 3-propargyl-3H-benzo[e]perimidine-2,7-diones were synthesized from 1-iodoanthraquinone. The propargyl derivative was subjected to Mannich and cycloaddition reactions.

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