Home / Publications / A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine

A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine

Igor Ivanovich Barabanov 1
Igor Ivanovich Barabanov
Irina Dmitrievna Ivanchikova 1
Irina Dmitrievna Ivanchikova
Mark Samuilovich Shvartsberg 1
Mark Samuilovich Shvartsberg
Published 2000-10-13
CommunicationVolume 10, Issue 5, 188-190
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Barabanov I. I., Ivanchikova I. D., Shvartsberg M. S. A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine // Mendeleev Communications. 2000. Vol. 10. No. 5. pp. 188-190.
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Barabanov I. I., Ivanchikova I. D., Shvartsberg M. S. A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine // Mendeleev Communications. 2000. Vol. 10. No. 5. pp. 188-190.
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TY - JOUR
DO - 10.1070/MC2000v010n05ABEH001353
UR - https://mendcomm.colab.ws/publications/10.1070/MC2000v010n05ABEH001353
TI - A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine
T2 - Mendeleev Communications
AU - Barabanov, Igor Ivanovich
AU - Ivanchikova, Irina Dmitrievna
AU - Shvartsberg, Mark Samuilovich
PY - 2000
DA - 2000/10/13
PB - Mendeleev Communications
SP - 188-190
IS - 5
VL - 10
ER -
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@article{2000_Barabanov,
author = {Igor Ivanovich Barabanov and Irina Dmitrievna Ivanchikova and Mark Samuilovich Shvartsberg},
title = {A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine},
journal = {Mendeleev Communications},
year = {2000},
volume = {10},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2000v010n05ABEH001353},
number = {5},
pages = {188--190},
doi = {10.1070/MC2000v010n05ABEH001353}
}
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Barabanov, Igor Ivanovich, et al. “A directive effect of heterofunctions in cyclocondensation reactions of acetylenylquinones with hydrazine.” Mendeleev Communications, vol. 10, no. 5, Oct. 2000, pp. 188-190. https://mendcomm.colab.ws/publications/10.1070/MC2000v010n05ABEH001353.

Abstract

The heterocycle formed in the cyclocondensation reactions of 2-acetylenyl-1-chloro-9,10-anthraquinones or 5-acetylenyl-3-diethylamino-1,4-naphthoquinones with NH2NH2 is influenced by the presence of a heterofunction, e.g. a hydroxyl group, in the acetylenic substituent; this directive effect was used for the synthesis of naphtho[2,3-h]cinnoline-4,7,12-trione and 4H-naphtho[1,8-cd]-1,2- diazepin-8-one derivatives.

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