Home / Publications / Synthesis of 4-haloquinolines and their fused polycyclic derivatives

Synthesis of 4-haloquinolines and their fused polycyclic derivatives

Mark Samuilovich Shvartsberg 1
Mark Samuilovich Shvartsberg
, 
Ekaterina A Kolodina 1
Ekaterina A Kolodina
10.1016/j.mencom.2008.03.020
Published 2008-03-18
Communication , Volume 18, Issue 2, 109-111
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Shvartsberg M. S., Kolodina E. A. Synthesis of 4-haloquinolines and their fused polycyclic derivatives // Mendeleev Communications. 2008. Vol. 18. No. 2. pp. 109-111.
GOST all authors (up to 50) Copy
Shvartsberg M. S., Kolodina E. A. Synthesis of 4-haloquinolines and their fused polycyclic derivatives // Mendeleev Communications. 2008. Vol. 18. No. 2. pp. 109-111.
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TY - JOUR
DO - 10.1016/j.mencom.2008.03.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.03.020
TI - Synthesis of 4-haloquinolines and their fused polycyclic derivatives
T2 - Mendeleev Communications
AU - Shvartsberg, Mark Samuilovich
AU - Kolodina, Ekaterina A
PY - 2008
DA - 2008/03/18
PB - Mendeleev Communications
SP - 109-111
IS - 2
VL - 18
ER -
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@article{2008_Shvartsberg,
author = {Mark Samuilovich Shvartsberg and Ekaterina A Kolodina},
title = {Synthesis of 4-haloquinolines and their fused polycyclic derivatives},
journal = {Mendeleev Communications},
year = {2008},
volume = {18},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.03.020},
number = {2},
pages = {109--111},
doi = {10.1016/j.mencom.2008.03.020}
}
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Shvartsberg, Mark Samuilovich, and Ekaterina A Kolodina. “Synthesis of 4-haloquinolines and their fused polycyclic derivatives.” Mendeleev Communications, vol. 18, no. 2, Mar. 2008, pp. 109-111. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.03.020.

Abstract

A general method for the synthesis of 4-chloro- or 4-bromo-substituted quinolines and quinoline moieties of polycyclic compounds includes the addition of hydrogen halides to vic-amino(3-oxoalk-1-ynyl)arenes under mild conditions followed by the intramolecular cyclization of the adducts.

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