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Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition
Burilov V., Epifanova N., Popova E., Vasilevsky S., Solovieva S., Antipin I., Konovalov A.
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on the 1,3-dipolar
The Reactivity of Addends in the 1,3-Dipolar Cycloaddition Reaction
Samuilov Y., Konovalov A.
in the 1,3-dipolar cycloaddition reaction is examined. It is shown that the interactions between
Mechanistic investigation of 1,3-dipolar cycloaddition between bifunctional 2-pyridylselenyl reagents and nitriles including reactions with cyanamides
Artemjev A.A., Kubasov A.S., Kuznetsov M.L., Grudova M.V., Khrustalev V.N., Kritchenkov A.S., Tskhovrebov A.G.
with an estimated interaction energy of −3.9 kcal mol−1, as revealed by theoretical calculations. Importantly
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition
Burilov V., Epifanova N., Popova E., Vasilevsky S., Solovieva S., Antipin I., Konovalov A.
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on the 1,3-dipolar
Facile synthesis of hydantoin/1,2,4-oxadiazoline spiro- compounds via 1,3-dipolar cycloaddition of nitrile oxides to 5-iminohydantoins
Petrova J.V., Tkachenko V.T., Tafeenko V.A., Pestretsova A.S., Pokrovsky V.S., Kukushkin M.E., Beloglazkina E.K.
of novel hydantoin/1,2,4-oxadiazoline spiro-compounds using a 1,3-dipolar cycloaddition of nitrile oxides
The Reactivity of Addends in the 1,3-Dipolar Cycloaddition Reaction
Samuilov Y., Konovalov A.
in the 1,3-dipolar cycloaddition reaction is examined. It is shown that the interactions between
1,3-Dipolar Cycloaddition of Nitrile Oxides and Nitrilimines to (−)-β-Caryophyllene: Stereoselective Synthesis of Polycyclic Derivatives and Their Biological Testing
Shybanov D.E., Kukushkin M.E., Grishin Y.K., Roznyatovsky V.A., Tafeenko V.A., Abo Qoura L., Pokrovsky V.S., Yarovaya O.I., Belyaevskaya S.V., Volobueva A.S., Esaulkova I.L., Zarubaev V.V., Beloglazkina E.K.
into the structure of sesquiterpenes by the 1,3-dipolar cycloaddition reactions of nitrile oxides and nitrilimines
1,3-Dipolar cycloaddition of C-Benzoyl-N-phenyl- and C,N-diphenylnitrones to β-substituted vinylphosphonates
Arbuzov B., Lisin A., Dianova E., Samitov Y.
1. The 1,3-dipolar cycloaddition of C,N-diphenyl- and C-benzoyl-N-phenylnitrones to diethyl β
Bifunctional derivatives of (Thia)calix[4]arenes with terminal double and triple bonds: Synthesis and azide-alkyne click reactions
Burilov V., Nugmanov R., Popova E., Nabiullin I., Soloviev S., Antipin I., Konovalov A.
bonds of the synthesized bifunctional compounds readily undergo Cu(I)-catalyzed 1,3-dipolar
Enantiomerically enriched 1,2-P,N-bidentate ferrocenyl ligands for 1,3-dipolar cycloaddition and transfer hydrogenation reactions
Utepova I.A., Serebrennikova P.O., Streltsova M.S., Musikhina A.A., Fedorchenko T.G., Chupakhin O.N., Antonchick A.P.
Novel complexes of 1,2-P,N-bidentate ferrocenyl ligands with AgOAc or with [RuCl2(PPh3)3

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