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Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones

Mark Samuilovich Shvartsberg 1
Mark Samuilovich Shvartsberg
, 
Igor Ivanovich Barabanov 1
Igor Ivanovich Barabanov
, 
Lidiya Georgievna Fedenok 1
Lidiya Georgievna Fedenok
10.1070/MC1997v007n03ABEH000762
Published 1997-06-30
Communication , Volume 7, Issue 3, 98-99
6
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Shvartsberg M. S., Barabanov I. I., Fedenok L. G. Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones // Mendeleev Communications. 1997. Vol. 7. No. 3. pp. 98-99.
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Shvartsberg M. S., Barabanov I. I., Fedenok L. G. Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones // Mendeleev Communications. 1997. Vol. 7. No. 3. pp. 98-99.
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TY - JOUR
DO - 10.1070/MC1997v007n03ABEH000762
UR - https://mendcomm.colab.ws/publications/10.1070/MC1997v007n03ABEH000762
TI - Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones
T2 - Mendeleev Communications
AU - Shvartsberg, Mark Samuilovich
AU - Barabanov, Igor Ivanovich
AU - Fedenok, Lidiya Georgievna
PY - 1997
DA - 1997/06/30
PB - Mendeleev Communications
SP - 98-99
IS - 3
VL - 7
ER -
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@article{1997_Shvartsberg,
author = {Mark Samuilovich Shvartsberg and Igor Ivanovich Barabanov and Lidiya Georgievna Fedenok},
title = {Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones},
journal = {Mendeleev Communications},
year = {1997},
volume = {7},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1997v007n03ABEH000762},
number = {3},
pages = {98--99},
doi = {10.1070/MC1997v007n03ABEH000762}
}
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Shvartsberg, Mark Samuilovich, et al. “Acetylenic compounds as key intermediates in heterocyclic synthesis: a route to functionalized naphtha[2,3-h]quinoline-7,12-diones.” Mendeleev Communications, vol. 7, no. 3, Jun. 1997, pp. 98-99. https://mendcomm.colab.ws/publications/10.1070/MC1997v007n03ABEH000762.

Abstract

Addition of primary and secondary amines to ethyl (1-amino-9,10-anthraquinon-2-yl)propiolate and cyclization of the resulting adducts to 2-substituted 4-dialkyl(or alkyl)aminonaphtho[2,3-h]quinoline-7,12-diones and 4-dialkyl(or alkyl)amino-1,2-dihydronaphtho[2,3-h]quinoline-2,7,12-triones are reported.

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