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Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols

Ravil Ismagilovich Khusnutdinov 1
Ravil Ismagilovich Khusnutdinov
, 
Alfiya Ruslanovna Bayguzina 1
Alfiya Ruslanovna Bayguzina
, 
Kirill Yu Denisov 1
Kirill Yu Denisov
, 
10.1016/j.mencom.2015.05.021
Published 2015-04-28
Communication , Volume 25, Issue 3, 219-220
5
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Khusnutdinov R. I. et al. Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 219-220.
GOST all authors (up to 50) Copy
Khusnutdinov R. I., Bayguzina A. R., Denisov K. Yu., Dzhemilev U. M. Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 219-220.
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TY - JOUR
DO - 10.1016/j.mencom.2015.05.021
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.021
TI - Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols
T2 - Mendeleev Communications
AU - Khusnutdinov, Ravil Ismagilovich
AU - Bayguzina, Alfiya Ruslanovna
AU - Denisov, Kirill Yu
AU - Dzhemilev, Usein Memetovich
PY - 2015
DA - 2015/04/28
PB - Mendeleev Communications
SP - 219-220
IS - 3
VL - 25
ER -
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@article{2015_Khusnutdinov,
author = {Ravil Ismagilovich Khusnutdinov and Alfiya Ruslanovna Bayguzina and Kirill Yu Denisov and Usein Memetovich Dzhemilev},
title = {Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.021},
number = {3},
pages = {219--220},
doi = {10.1016/j.mencom.2015.05.021}
}
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Khusnutdinov, Ravil Ismagilovich, et al. “Synthesis of phenanthrene-9-carboxylic esters by the iron-catalyzed reaction of phenanthrene with CCl4 and alcohols.” Mendeleev Communications, vol. 25, no. 3, Apr. 2015, pp. 219-220. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.021.

Abstract

Alkyl phenanthrene-9-carboxylates were synthesized in 74–96% yields by the iron-catalyzed reaction of phenanthrene with tetrachloromethaneand alkanols

References

1.
E. Gellert, in Alkaloids: Chemical and Biological Perspectives, ed. S. W. Pelletier, Academic Press, New York, 1987, pp. 55-132.
2.
M. Suffness and G. A. Cordell, in The Alkaloids, Chemistry and Pharmacology, ed. A. Brossi, Academic Press, New York, 1987, pp. 3-355.
3.
Antimalarial arylaminopropanols
Colwell W.T., Brown V., Christie P., Lange J., Reece C., Yamamoto K., Henry D.W.
Journal of Medicinal Chemistry, 1972
4.
Design, Synthesis, and Antiviral Evaluation of Phenanthrene-Based Tylophorine Derivatives as Potential Antiviral Agents
Wang K., Hu Y., Liu Y., Mi N., Fan Z., Liu Y., Wang Q.
Journal of Agricultural and Food Chemistry, 2010
5.
Excimer fluorescence from phenanthrene-9-carboxylate derivatives
Lewis F.D., Burch E.L.
Journal of Photochemistry and Photobiology A: Chemistry, 1996
6.
Photoluminescence Studies of Phenanthrene−Azomethyne Conjugated−Nonconjugated Multiblock Copolymer
Machado A.M., Munaro M., Martins T.D., Dávila L.Y., Giro R., Caldas M.J., Atvars T.D., Akcelrud L.C.
Macromolecules, 2006
8.
Lewis Acid-Mediated Carboxylation of Fused Aromatic Compounds with Carbon Dioxide
Suzuki Y., Hattori T., Okuzawa T., Miyano S.
Chemistry Letters, 2002
9.
Direct Carboxylation of Arenes and Halobenzenes with CO2 by the Combined Use of AlBr3 and R3SiCl
Nemoto K., Yoshida H., Egusa N., Morohashi N., Hattori T.
Journal of Organic Chemistry, 2010
10.
Photochemical and Photophysical Behavior ofp-Methoxyphenyl alkenyl Phenanthrenecarboxylates. I. Structure and Competitive Formation of Intramolecular Cycloaddition Products
Sakuragi H., Tokumaru K., Itoh H., Terakawa K., Kikuchi K., Caldwell R.A., Hsu C.
Bulletin of the Chemical Society of Japan, 1990
13.
Direct One-Pot Synthesis of Phenanthrenes via Suzuki−Miyaura Coupling/Aldol Condensation Cascade Reaction
Kim Y.H., Lee H., Kim Y.J., Kim B.T., Heo J.
Journal of Organic Chemistry, 2007
14.
A short history of SHELX
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography, 2007
15.
Electrophilic aromatic trichloromethylation: intermediates and products
Belen"kii L.I., Chuvylkin N.D., Suslov I.A.
Russian Chemical Bulletin, 2001
16.
10.1016/j.mencom.2015.05.021_bib0080
Belen’kii
Chem. Scripta, 1989
17.
Some Reactions of the Trifluoromethyl Group in the Benzotrifluoride Series. II. Alcoholysis1
Fave G.M., Scheurer P.G.
Journal of the American Chemical Society, 1950