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A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones

Maxim Sergeyevich Slezkin 1
Maxim Sergeyevich Slezkin
Sergey Nikolaevich Mantrov 1
Sergey Nikolaevich Mantrov
Published 2009-05-08
CommunicationVolume 19, Issue 3, 159-160
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Slezkin M. S., Mantrov S. N. A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones // Mendeleev Communications. 2009. Vol. 19. No. 3. pp. 159-160.
GOST all authors (up to 50) Copy
Slezkin M. S., Mantrov S. N. A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones // Mendeleev Communications. 2009. Vol. 19. No. 3. pp. 159-160.
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TY - JOUR
DO - 10.1016/j.mencom.2009.05.016
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.05.016
TI - A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones
T2 - Mendeleev Communications
AU - Slezkin, Maxim Sergeyevich
AU - Mantrov, Sergey Nikolaevich
PY - 2009
DA - 2009/05/08
PB - Mendeleev Communications
SP - 159-160
IS - 3
VL - 19
ER -
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@article{2009_Slezkin,
author = {Maxim Sergeyevich Slezkin and Sergey Nikolaevich Mantrov},
title = {A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones},
journal = {Mendeleev Communications},
year = {2009},
volume = {19},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.05.016},
number = {3},
pages = {159--160},
doi = {10.1016/j.mencom.2009.05.016}
}
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Slezkin, Maxim Sergeyevich, and Sergey Nikolaevich Mantrov. “A new protocol for the construction of pyrrolo[4,3,2-de]quinolinones.” Mendeleev Communications, vol. 19, no. 3, May. 2009, pp. 159-160. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.05.016.

Abstract

A facile method has been suggested for constructing pyrrolo[4,3,2-de]quinolinones by addition of acetophenones to 4-nitroisatin followed by reduction of the nitro group and spontaneous cyclisation.

References

2.
V. G. Kartsev, Izbrannye metody sinteza i modifikatsii geterotsiklov (Selected Methods of Synthesis and Modification of Heterocycles), IBS Press, Moscow, 2004, vol. 3, p. 472. (in Russian).
3.
A. Kleeman and J. Engel, Pharmazeutische Wirkstoffe. Synthesen, Patente, Anwendungen, Georg Thieme Verlag, Stuttgart–New York, 1982, p. 47.
5.
Crystal-structure-based design and synthesis of benz[cd]indole-containing inhibitors of thymidylate synthase
Varney M.D., Marzoni G.P., Palmer C.L., Deal J.G., Webber S., Welsh K.M., Bacquet R.J., Bartlett C.A., Morse C.A.
Journal of Medicinal Chemistry, 1992
6.
T. Akama and H. Nagata, US Patent, 6613774, B1, 2003.
7.
Synthesis of 2-Methyl-3-quinolinol Derivatives.
Goto T., Ilirata Y.
Nippon kagaku zassi, 1954
8.
Synthesis of Some Pyrrolo[4,3,2-de]quinolines
Balczewski P., Joule J.A., Estevez C., Alvarez M.
Journal of Organic Chemistry, 1994
9.
10.1016/j.mencom.2009.05.016_bib9
Mercedes
Eur. J. Org. Chem., 1999
10.
The first total synthesis of lymphostin
Tatsuta K., Imamura K., Itoh S., Kasai S.
Tetrahedron Letters, 2004
11.
10.1016/j.mencom.2009.05.016_bib11
Shvekhgeimer
Khim. Geterotsikl. Soedin., 1996
12.
A general method for the synthesis of isatins
Gassman P.G., Cue B.W., Luh T.
Journal of Organic Chemistry, 1977