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An efficient approach to isoindolo[2,1-b][2]benzazepines via intramolecular [4+2] cycloaddition of maleic anhydride to 4-alpha-furyl-4-N-benzylaminobut-1-enes
Zubkov F.I., Boltukhina E.V., Turchin K.F., Varlamov A.V.
-Alder reaction of furan (IMDAF). The cycloaddition proceeded under mild reaction conditions (25 degrees
Novel Highly Efficient Green and Reusable Cu(II)/Chitosan-Based Catalysts for the Sonogashira, Buchwald, Aldol, and Dipolar Cycloaddition Reactions
Dysin A.P., Egorov A.R., Khubiev O, Golubev R, Kirichuk A.A., Khrustalev V.N., Lobanov N.N., Rubanik V.V., Tskhovrebov A.G., Kritchenkov A.S.
cycloaddition. The elaborated catalytic systems efficiently catalyze the aforementioned reactions
[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones
Kuznetsova Juliana V., Tkachenko Varvara T., Petrovskaya Lada M., Filkina Maria E., Shybanov Dmitry E., Grishin Yuri K., Roznyatovsky Vitaly A., Tafeenko Viktor A., Pestretsova Anna S., Yakovleva Vera A., Pokrovsky Vadim S., Kukushkin Maxim E., Beloglazkina Elena K.
Approximately 1,3-Dipolar cycloaddition of imidazolidine derivatives containing exocyclic double
Asymmetric Metal‐Templated Approach to Amino Acids with a CF3‐Containing 3,2’‐Pyrrolidinyl Spirooxindole Core via a Michael/Mannich [3+2]‐Cycloaddition Reaction
Gugkaeva Zalina T., Stukalova Maria P., Smol'yakov Alexander F., Tsaloev Alan T., Maleev Victor I., Larionov Vladimir A.
with three defined carbon stereocenters via a sequential Michael/Mannich [3+2]‐cycloaddition reaction
Solvent Free Ambient Pressure CO2 Cycloaddition Catalyzed by Cobalt-Impregnated 2D-Nanofibrous COFs
Ullah H., Ullah Z., Khattak Z.A.K., Tahir M., Kang E., Verpoort F., You Kim H.
coupling at ambient pressure. We found that the Co2+ ions within the COF matrix catalyze CO2 cycloaddition
[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives-An Approach to Novel Spiroimidazolidinediones
Kuznetsova J.V., Tkachenko V.T., Petrovskaya L.M., Filkina M.E., Shybanov D.E., Grishin Y.K., Roznyatovsky V.A., Tafeenko V.A., Pestretsova A.S., Yakovleva V.A., Pokrovsky V.S., Kukushkin M.E., Beloglazkina E.K.
Approximately 1,3-Dipolar cycloaddition of imidazolidine derivatives containing exocyclic
5-amido- and 5-amino-substituted epoxyisoindolo[2,1-a]tetrahydroquinolines and 10-carboxylic acids: Their synthesis and reactivity
Zaytsev V.P., Zubkov F.I., Toze F.A.A., Orlova D.N., Eliseeva M.N., Grudinin D.G., Nikitina E.V., Varlamov A.V.
by a spontaneous [4+2]-cycloaddition of an N-acryloyl substituent to the furan ring. It was established
Ring-chain tautomerism in the products of the reaction between 5-substituted furfurylamines and anhydrides of α,β-unsaturated carboxylic acids
Zubkov F.I., Golubev V.D., Zaytsev V.P., Bakhanovich O.V., Nikitina E.V., Khrustalev V.N., Aysin R.R., Timofeeva T.V., Novikov R.A., Varlamov A.V.
formed a dynamic equilibrium in solutions with adducts formed by intramolecular [4+2] cycloaddition, 3a,6
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: Kinetic: versus thermodynamic control
Borisova K.K., Nikitina E.V., Novikov R.A., Khrustalev V.N., Dorovatovskii P.V., Zubavichus Y.V., Kuznetsov M.L., Zaytsev V.P., Varlamov A.V., Zubkov F.I.
The tandem [4+2] cycloaddition between hexafluoro-2-butyne and bis-furyl dienes, like difurfuryl
The intramolecular Diels-Alder vinylthiophen (IMDAV) reaction: An easy approach to thieno[2,3-f]isoindole-4-carboxylic acids
Horak Y.I., Lytvyn R.Z., Laba Y.-O.V., Homza Y.V., Zaytsev V.P., Nadirova M.A., Nikanorova T.V., Zubkov F.I., Varlamov A.V., Obushak M.D.
domino sequence involving successive acylation/[4+2] cycloaddition steps, leads to the formation

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