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Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines

Aleksandr Vladimirovich Piskunov 1
Aleksandr Vladimirovich Piskunov
, 
Mark Samuilovich Shvartsberg 1
Mark Samuilovich Shvartsberg
10.1070/MC1995v005n04ABEH000504
Published 1995-08-31
Communication , Volume 5, Issue 4, 155-156
7
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Piskunov A. V., Shvartsberg M. S. Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines // Mendeleev Communications. 1995. Vol. 5. No. 4. pp. 155-156.
GOST all authors (up to 50) Copy
Piskunov A. V., Shvartsberg M. S. Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines // Mendeleev Communications. 1995. Vol. 5. No. 4. pp. 155-156.
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TY - JOUR
DO - 10.1070/MC1995v005n04ABEH000504
UR - https://mendcomm.colab.ws/publications/10.1070/MC1995v005n04ABEH000504
TI - Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines
T2 - Mendeleev Communications
AU - Piskunov, Aleksandr Vladimirovich
AU - Shvartsberg, Mark Samuilovich
PY - 1995
DA - 1995/08/31
PB - Mendeleev Communications
SP - 155-156
IS - 4
VL - 5
ER -
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@article{1995_Piskunov,
author = {Aleksandr Vladimirovich Piskunov and Mark Samuilovich Shvartsberg},
title = {Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines},
journal = {Mendeleev Communications},
year = {1995},
volume = {5},
publisher = {Mendeleev Communications},
month = {Aug},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1995v005n04ABEH000504},
number = {4},
pages = {155--156},
doi = {10.1070/MC1995v005n04ABEH000504}
}
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Piskunov, Aleksandr Vladimirovich, and Mark Samuilovich Shvartsberg. “Cyclization of Adducts of 1-Amino-2-ethynylanthraquinone and Secondary Amines.” Mendeleev Communications, vol. 5, no. 4, Aug. 1995, pp. 155-156. https://mendcomm.colab.ws/publications/10.1070/MC1995v005n04ABEH000504.

Abstract

Adducts of 1-amino-2-ethynylanthraquinone and secondary amines are cyclized to 2-dialkylamino-2,3-dihydronaphtho[2,3-g]indole-6,11-dionesand subsequently, depending on the reaction conditions, are either deaminated to naphtha[2,3-g]indole-6,11-dione or dehydrogenated to its 2-dialkyiamino derivatives.

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