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Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles

Galina Vyacheslavovna Kokurkina 1
Galina Vyacheslavovna Kokurkina
Mikhail Dmitrievich Dutov 1
Mikhail Dmitrievich Dutov
Svyatoslav Arkad'evich Shevelev 1
Svyatoslav Arkad'evich Shevelev
Bogdan Ivanovich Ugrak 1
Bogdan Ivanovich Ugrak
Published 2011-07-01
CommunicationVolume 21, Issue 4, 196-197
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Kokurkina G. V. et al. Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles // Mendeleev Communications. 2011. Vol. 21. No. 4. pp. 196-197.
GOST all authors (up to 50) Copy
Kokurkina G. V., Dutov M. D., Shevelev S. A., Ugrak B. I. Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles // Mendeleev Communications. 2011. Vol. 21. No. 4. pp. 196-197.
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TY - JOUR
DO - 10.1016/j.mencom.2011.07.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.008
TI - Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles
T2 - Mendeleev Communications
AU - Kokurkina, Galina Vyacheslavovna
AU - Dutov, Mikhail Dmitrievich
AU - Shevelev, Svyatoslav Arkad'evich
AU - Ugrak, Bogdan Ivanovich
PY - 2011
DA - 2011/07/01
PB - Mendeleev Communications
SP - 196-197
IS - 4
VL - 21
ER -
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@article{2011_Kokurkina,
author = {Galina Vyacheslavovna Kokurkina and Mikhail Dmitrievich Dutov and Svyatoslav Arkad'evich Shevelev and Bogdan Ivanovich Ugrak},
title = {Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.008},
number = {4},
pages = {196--197},
doi = {10.1016/j.mencom.2011.07.008}
}
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Kokurkina, Galina Vyacheslavovna, et al. “Intramolecular cyclization of O-(3,5-diaminophenyl)-substituted ketoximes as a route to 6-amino-4-hydroxyindoles.” Mendeleev Communications, vol. 21, no. 4, Jul. 2011, pp. 196-197. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.008.

Abstract

O-(3,5-Diaminophenyl)-substituted ketoximes undergo acid-catalysed cyclization to afford 6-amino-4-hydroxyindoles.

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