Home / Publications / Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride

Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride

Alexey N Yamskov 1
Alexey N Yamskov
Alexander Viktorovich Samet 1
Alexander Viktorovich Samet
Victor Vladimirovich Semenov 1
Victor Vladimirovich Semenov
Published 2008-11-01
CommunicationVolume 18, Issue 6, 320-321
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Yamskov A. N., Samet A. V., Semenov V. V. Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride // Mendeleev Communications. 2008. Vol. 18. No. 6. pp. 320-321.
GOST all authors (up to 50) Copy
Yamskov A. N., Samet A. V., Semenov V. V. Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride // Mendeleev Communications. 2008. Vol. 18. No. 6. pp. 320-321.
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TY - JOUR
DO - 10.1016/j.mencom.2008.11.011
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.11.011
TI - Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride
T2 - Mendeleev Communications
AU - Yamskov, Alexey N
AU - Samet, Alexander Viktorovich
AU - Semenov, Victor Vladimirovich
PY - 2008
DA - 2008/11/01
PB - Mendeleev Communications
SP - 320-321
IS - 6
VL - 18
ER -
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@article{2008_Yamskov,
author = {Alexey N Yamskov and Alexander Viktorovich Samet and Victor Vladimirovich Semenov},
title = {Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride},
journal = {Mendeleev Communications},
year = {2008},
volume = {18},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.11.011},
number = {6},
pages = {320--321},
doi = {10.1016/j.mencom.2008.11.011}
}
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Yamskov, Alexey N., et al. “Preparation of benzoannulated seven- and eight-membered heterocycles from 2,4,6-trinitrobenzoyl chloride.” Mendeleev Communications, vol. 18, no. 6, Nov. 2008, pp. 320-321. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.11.011.

Abstract

Dinitro-substituted 1,2,3-triazolo[1,5-a]dibenzo[b,f][1,4]diazepin-7-one and 10,11-dihydro-11-(4-chlorophenyl)dibenz[b,g]-[1,5]oxazocin-12-one were prepared in two steps from 2,4,6-trinitrobenzoyl chloride.

References

1.
Aromatic nucleophilic denitrocyclization reactions
3.
Abramov I.G., Smirnov A.V., Ivanovskii S.A., Abramova M.B., Plakhtinskii V.V., Belysheva M.S.
Mendeleev Communications, 2001
4.
Synthesis of Substituted Dibenz-oxazepines and Dibenzthiazepine Using of 4-Bromo-5-nitrophthalonitrile
G. Abramov I., V. Smirnov A., S. Kalandadze L., N. Sakharov V., V. Plakhtinskii V.
Heterocycles, 2003
5.
Smirnov A.V., Kalandadze L.S., Sakharov V.N., Dorogov M.V.
Mendeleev Communications, 2006
7.
10.1016/j.mencom.2008.11.011_bib7
Samet
Izv. Akad. Nauk, Ser. Khim., 2006
8.
4, 5-Dihydro-1, 4-benzoxazepin-3(2H)-ones
Derieg M.E., Sternbach L.H.
Journal of Heterocyclic Chemistry, 1966