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Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes

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Kulikova L. N., Borisov R. S., Voskresenskii L. G. Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 640-641.
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Kulikova L. N., Borisov R. S., Voskresenskii L. G. Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 640-641.
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TY - JOUR
DO - 10.1016/j.mencom.2017.11.035
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.035
TI - Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes
T2 - Mendeleev Communications
AU - Kulikova, Larisa Nikolaevna
AU - Borisov, Roman Sergeevich
AU - Voskresenskii, Leonid Gennadievich
PY - 2017
DA - 2017/10/30
PB - Mendeleev Communications
SP - 640-641
IS - 6
VL - 27
ER -
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@article{2017_Kulikova,
author = {Larisa Nikolaevna Kulikova and Roman Sergeevich Borisov and Leonid Gennadievich Voskresenskii},
title = {Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.035},
number = {6},
pages = {640--641},
doi = {10.1016/j.mencom.2017.11.035}
}
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Kulikova, Larisa Nikolaevna, et al. “Ring opening in 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines under the action of electron-deficient alkynes.” Mendeleev Communications, vol. 27, no. 6, Oct. 2017, pp. 640-641. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.035.

Abstract

2-Vinyl substituted chromones were obtained by the reaction between 1,2,3,4-tetrahydrochromeno[3,2-c]pyridines and electron-deficient alkynes.

References

2.
Novel CFTR Chloride Channel Activators Identified by Screening of Combinatorial Libraries Based on Flavone and Benzoquinolizinium Lead Compounds
Galietta L.J., Springsteel M.F., Eda M., Niedzinski E.J., By K., Haddadin M.J., Kurth M.J., Nantz M.H., Verkman A.S.
Journal of Biological Chemistry, 2001
3.
Refinement and Evaluation of a Pharmacophore Model for Flavone Derivatives Binding to the Benzodiazepine Site of the GABAA Receptor
Kahnberg P., Lager E., Rosenberg C., Schougaard J., Camet L., Sterner O., Nielsen E.Ø., Nielsen M., Liljefors T.
Journal of Medicinal Chemistry, 2002
4.
Flavonoids and their glycosides, including anthocyanins
Veitch N.C., Grayer R.J.
Natural Product Reports, 2008
5.
β-Naphthoflavone analogs as potent and soluble aryl hydrocarbon receptor agonists: Improvement of solubility by disruption of molecular planarity
Fujita Y., Yonehara M., Tetsuhashi M., Noguchi-Yachide T., Hashimoto Y., Ishikawa M.
Bioorganic and Medicinal Chemistry, 2010
6.
Efficient Synthesis of Arylated Flavones by Site‐Selective Suzuki–Miyaura Cross‐Coupling Reactions of the Bis(triflate) of 5,7‐ and 7,8‐Dihydroxyflavone
Eleya N., Malik I., Reimann S., Wittler K., Hein M., Patonay T., Villinger A., Ludwig R., Langer P.
European Journal of Organic Chemistry, 2012
7.
Antimalarials from nature
Kaur K., Jain M., Kaur T., Jain R.
Bioorganic and Medicinal Chemistry, 2009
9.
Chromone: a valid scaffold in medicinal chemistry.
Gaspar A., Matos M.J., Garrido J., Uriarte E., Borges F.
Chemical Reviews, 2014
11.
Kornev M.Y., Moshkin V.S., Eltsov O.S., Sosnovskikh V.Y.
Mendeleev Communications, 2016
13.
Synthesis of Novel Tricyclic Chromenone-Based Inhibitors of IRE-1 RNase Activity
Ranatunga S., Tang C.A., Kang C.W., Kriss C.L., Kloppenburg B.J., Hu C.A., Del Valle J.R.
Journal of Medicinal Chemistry, 2014
14.
The reaction of tetrahydrochromeno[3,4-c]pyridines with activated alkynes. The first synthesis of tetrahydrochromeno[4,3-d]azocines
Voskressensky L.G., Kulikova L.N., Gozun S.V., Khrustalev V.N., Borisova T.N., Listratova A.V., Ovcharov M.V., Varlamov A.V.
Tetrahedron Letters, 2011
15.
Synthesis of new fundamental heterocycles. Part VII. Synthesis of 2‐azaxanthene
16.
OLEX2: a complete structure solution, refinement and analysis program
Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A., Puschmann H.
Journal of Applied Crystallography, 2009
17.
SHELXT– Integrated space-group and crystal-structure determination
Sheldrick G.M.
Acta Crystallographica Section A: Foundations and Advances, 2015
18.
Crystal structure refinement withSHELXL
Sheldrick G.M.
Acta crystallographica. Section C, Structural chemistry, 2015
19.
Single-crystal structure validation with the programPLATON
20.
Synthesis of 2-styrylchromones as a novel class of antiproliferative agents targeting carcinoma cells
Shaw A.Y., Chang C., Liau H., Lu P., Chen H., Yang C., Li H.
European Journal of Medicinal Chemistry, 2009
21.
Synthesis and anticancer activity of lavendustin A derivatives containing arylethenylchromone substituents
Lee K.Y., Nam D.H., Moon C.S., Seo S.H., Lee J.Y., Lee Y.S.
European Journal of Medicinal Chemistry, 2006