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Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature

, 
Fedor Vladimirovich Ryzhkov 1
Fedor Vladimirovich Ryzhkov
, 
Tatiana Aleksandrovna Zaimovskaya 2
Tatiana Aleksandrovna Zaimovskaya
, 
Mikhail Petrovich Egorov 1
Mikhail Petrovich Egorov
10.1016/j.mencom.2015.05.008
Published 2015-04-28
Communication , Volume 25, Issue 3, 185-187
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Elinson M. N. et al. Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 185-187.
GOST all authors (up to 50) Copy
Elinson M. N., Ryzhkov F. V., Zaimovskaya T. A., Egorov M. P. Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 185-187.
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TY - JOUR
DO - 10.1016/j.mencom.2015.05.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.008
TI - Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature
T2 - Mendeleev Communications
AU - Elinson, Michail Nikolaevich
AU - Ryzhkov, Fedor Vladimirovich
AU - Zaimovskaya, Tatiana Aleksandrovna
AU - Egorov, Mikhail Petrovich
PY - 2015
DA - 2015/04/28
PB - Mendeleev Communications
SP - 185-187
IS - 3
VL - 25
ER -
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@article{2015_Elinson,
author = {Michail Nikolaevich Elinson and Fedor Vladimirovich Ryzhkov and Tatiana Aleksandrovna Zaimovskaya and Mikhail Petrovich Egorov},
title = {Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.008},
number = {3},
pages = {185--187},
doi = {10.1016/j.mencom.2015.05.008}
}
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Elinson, Michail Nikolaevich, et al. “Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature.” Mendeleev Communications, vol. 25, no. 3, Apr. 2015, pp. 185-187. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.008.

Abstract

Non-catalytic solvent-free assembling of aldehydes, dimedone and malononitrile at ambient temperature affords substituted 5,6,7,8-tetrahydro-4H-chromenes in 88–98% yields.

References

1.
Multicomponent Reactions, eds. J. Zhu and H. Bienayme, Wiley-VCH, Weinheim, 2005.
2.
Multi-component syntheses of heterocycles by transition-metal catalysis.
D'Souza D.M., Müller T.J.
Chemical Society Reviews, 2007
3.
Synthesis of Heterocycles via Multicomponent Reactions I, eds. R. V. A. Orru and E. Ruijter, Springer, New York, 2010.
5.
Recent advances in isocyanide-based multicomponent chemistry
Dömling A.
Current Opinion in Chemical Biology, 2002
6.
Drug Design, ed. G. Klebe, Springer, Berlin, 2013.
9.
Synthesis and pharmacological activity of 2-oxo-(2H) 1-benzopyran-3-carboxamide derivatives
Bonsignore L., Loy G., Secci D., Calignano A.
European Journal of Medicinal Chemistry, 1993
10.
Phytochemistry of the genus Piper
Parmar V.S., Jain S.C., Bisht K.S., Jain R., Taneja P., Jha A., Tyagi O.D., Prasad A.K., Wengel J., Olsen C.E., Boll P.M.
Phytochemistry, 1997
11.
Chemical modification of the natural flavonoid myricetin
Polyakov V.V.
Chemistry of Natural Compounds, 1999
12.
10.1016/j.mencom.2015.05.008_bib0060
Konkoy
PCT Int. Appl. WO 0075123, 2000
13.
10.1016/j.mencom.2015.05.008_bib0065
Abdel-Latif
J. Chem. Res. Miniprint, 1995
14.
10.1016/j.mencom.2015.05.008_bib0070
Hassanien
J. Indian Chem. Soc., 1999
22.
Electrogenerated base-promoted synthesis of tetrahydrobenzo[b]pyran derivatives
Fotouhi L., Heravi M.M., Fatehi A., Bakhtiari K.
Tetrahedron Letters, 2007
23.
The Implication of Electrocatalysis in MCR Strategy: Electrocatalytic Multicomponent Transformation of Cyclic 1,3-Diketones, Aldehydes and Malononitrile into Substituted 5,6,7,8-Tetrahydro-4H-Chromenes
Elinson M.N., Dorofeev A.S., Feducovich S.K., Gorbunov S.V., Nasybullin R.F., Miloserdov F.M., Nikishin G.I.
European Journal of Organic Chemistry, 2006
28.
Elinson M.N., Medvedev M.G., Ilovaisky A.I., Merkulova V.M., Zaimovskaya T.A., Nikishin G.I.
Mendeleev Communications, 2013
34.
Elinson M.N., Ilovaisky A.I., Merkulova V.M., Zaimovskaya T.A., Nikishin G.I.
Mendeleev Communications, 2012
35.
Elinson M.N., Sokolova O.O., Nasybullin R.F., Zaimovskaya T.A., Egorov M.P.
Mendeleev Communications, 2015