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Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines

Albert Faridovich Khasanov 1
Albert Faridovich Khasanov
, 
Dmitrii Sergeevich Kopchuk 1, 2
Dmitrii Sergeevich Kopchuk
, 
Igor Sergeevich Kovalev 1
Igor Sergeevich Kovalev
, 
Olga Sergeevna Taniya 1
Olga Sergeevna Taniya
, 
Grigory Vasil'evich Zyryanov 1, 2
Grigory Vasil'evich Zyryanov
, 
Vladimir Leonidovich Rusinov 1, 2
Vladimir Leonidovich Rusinov
, 
Oleg Nikolaevich Chupakhin 1, 2
Oleg Nikolaevich Chupakhin
10.1016/j.mencom.2015.09.003
Published 2015-09-10
Communication , Volume 25, Issue 5, 332-333
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Khasanov A. F. et al. Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines // Mendeleev Communications. 2015. Vol. 25. No. 5. pp. 332-333.
GOST all authors (up to 50) Copy
Khasanov A. F., Kopchuk D. S., Kovalev I. S., Taniya O. S., Zyryanov G. V., Rusinov V. L., Chupakhin O. N. Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines // Mendeleev Communications. 2015. Vol. 25. No. 5. pp. 332-333.
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TY - JOUR
DO - 10.1016/j.mencom.2015.09.003
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.09.003
TI - Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines
T2 - Mendeleev Communications
AU - Khasanov, Albert Faridovich
AU - Kopchuk, Dmitrii Sergeevich
AU - Kovalev, Igor Sergeevich
AU - Taniya, Olga Sergeevna
AU - Zyryanov, Grigory Vasil'evich
AU - Rusinov, Vladimir Leonidovich
AU - Chupakhin, Oleg Nikolaevich
PY - 2015
DA - 2015/09/10
PB - Mendeleev Communications
SP - 332-333
IS - 5
VL - 25
ER -
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@article{2015_Khasanov,
author = {Albert Faridovich Khasanov and Dmitrii Sergeevich Kopchuk and Igor Sergeevich Kovalev and Olga Sergeevna Taniya and Grigory Vasil'evich Zyryanov and Vladimir Leonidovich Rusinov and Oleg Nikolaevich Chupakhin},
title = {Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.09.003},
number = {5},
pages = {332--333},
doi = {10.1016/j.mencom.2015.09.003}
}
MLA
Cite this
MLA Copy
Khasanov, Albert Faridovich, et al. “Reaction of lithium 2-arylethynides with 6-aryl-3-(2-pyridyl)-1,2,4-triazines as an access to 6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines.” Mendeleev Communications, vol. 25, no. 5, Sep. 2015, pp. 332-333. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.09.003.

Abstract

Reaction of 6-aryl-3-(2-pyridyl)-1,2,4-triazines with lithium 2-arylethynides affords (E)-6-aryl-5-arylvinyl-3-(2-pyridyl)-1,2,4-triazines.

References

3.
Intramolecular diels-alder reactions of 1,2,4-triazines.
Taylor E.C., Macor J.E., Pont J.L.
Tetrahedron, 1987
4.
An intramolecular inverse electron demand Diels–Alder approach to annulated α-carbolines
Ma Z., Ni F., Woo G.H., Lo S., Roveto P.M., Schaus S.E., Snyder J.K.
Beilstein Journal of Organic Chemistry, 2012
5.
Synthesis of 3,4-dihydro-1,8-naphthyridin-2(1H)-ones via microwave-activated inverse electron-demand Diels–Alder reactions
Fadel S., Hajbi Y., Khouili M., Lazar S., Suzenet F., Guillaumet G.
Beilstein Journal of Organic Chemistry, 2014
8.
Copper on Iron: Catalyst and Scavenger for Azide–Alkyne Cycloaddition
Novák Z., Kovács S., Zih-Perényi K., Révész Á.
Synthesis, 2012
9.
A general purpose reporter for cations: absorption, fluorescence and electrochemical sensing of zinc(ii)
Benniston A.C., Harriman A., Lawrie D.J., Mayeux A., Rafferty K., Russell O.D.
Dalton Transactions, 2003
10.
Conjugated 1,10-Phenanthrolines as Tunable Fluorophores
Joshi H.S., Jamshidi R., Tor Y.
Angewandte Chemie - International Edition, 1999
11.
10.1016/j.mencom.2015.09.003_sbref0025a
Yamaguchi
J. Am. Chem. Soc., 2001
12.
10.1016/j.mencom.2015.09.003_sbref0025b
Yang
J. Am. Chem. Soc., 1998
13.
Structure—Property relationships for exciton transfer in conjugated polymers
Andrew T.L., Swager T.M.
Journal of Polymer Science, Part B: Polymer Physics, 2011
15.
10.1016/j.mencom.2015.09.003_sbref0030b
Karak
RSC Adv., 2014
17.
Recent advances in Sonogashira reactions
Chinchilla R., Nájera C.
Chemical Society Reviews, 2011
18.
Direct meso-Alkynylation of Porphyrins Doubly Assisted by Pyridyl Coordination
Anabuki S., Tokuji S., Aratani N., Osuka A.
Organic Letters, 2012
19.
(a) D. N. Kozhevnikov, V.N. Kozhevnikov, A.M. Prokhorov, M.M. Ustinova, V.L. Rusinov, O.N. Chupakhin, G.G. Aleksandrov and B. Köenig, Tetrahedron Lett., 2006, 47, 869; (b) A. M. Prokhorov, P.A. Slepukhin and D. N. Kozhevnikov, J. Organomet. Chem., 2008, 693, 1886.
20.
Direct introduction of acetylene moieties into azines by methodology
Prokhorov A.M., Mąkosza M., Chupakhin O.N.
Tetrahedron Letters, 2009
21.
10.1016/j.mencom.2015.09.003_bib0050
Chupakhin
Nucleophilic Aromatic Substitution of Hydrogen, 1994
23.
1,2,4-Triazine N-oxides
Kozhevnikov D.N., Rusinov V.L., Chupakhin O.N.
Advances in Heterocyclic Chemistry, 2002
25.
(a) V. N. Kozhevnikov, D. N. Kozhevnikov, T. V. Nikitina, V. L. Rusinov, O. N. Chupakhin, M. Zabel and B. König, J. Org. Chem., 2003, 68, 2882; (b) A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin, I. V. Glukhov, M. Yu. Antipin, O. N. Kazheva, A. N. Chekhlov and O. A. Dyachenko, Organometallics, 2006, 25, 2972; (c) I. S. Kovalev, D. S. Kopchuk, A. F. Khasanov, G. V. Zyryanov, V. L. Rusinov and O. N. Chupakhin, Mendeleev Commun., 2014, 24, 117.
26.
Synthesis and Pharmacological Evaluation of Phenylethynyl[1,2,4]methyltriazines as Analogues of 3-Methyl-6-(phenylethynyl)pyridine
Carroll F.I., Kotturi S.V., Navarro H.A., Mascarella S.W., Gilmour B.P., Smith F.L., Gabra B.H., Dewey W.L.
Journal of Medicinal Chemistry, 2007
29.
10.1016/j.mencom.2015.09.003_bib0090
Beveridge
Synthesis, 2010
30.
SnCl4-Promoted Ethenylation Reaction of Hydroxylated Heteroarenes
Yamaguchi M., Akamatsu K., Amemiya R.
Heterocycles, 2004
32.
[Ru(η5-C5H5)(η6-C10H8)]PF6as a catalyst precursor for the one-pot direct C–H alkenylation of nitrogen heterocycles
Lynam J.M., Milner L.M., Mistry N.S., Slattery J.M., Warrington S.R., Whitwood A.C.
Dalton Transactions, 2014
36.
KOtBu-mediated stereoselective addition of quinazolines to alkynes under mild conditions.
Zhao D., Shen Q., Zhou Y., Li J.
Organic and Biomolecular Chemistry, 2013