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Diels-Alder reaction between naphthalene and N-phenylmaleimide under mild conditions
Kiselev V., Kashaeva E., Potapova L., Iskhakova G.
The rate and equilibrium constants for the Diels-Alder reactions between benzene or naphthalene
Diels-Alder reaction volumes in the solid state and solution
Kiselev V., Iskhakova G., Kashaeva E., Potapova L., Konovalov A.
in dioxane, acetonitrile, and 1,2-dichloroethane, The experimental Diels-Alder reaction volumes in solution
Intramolecular [4+2] cycloaddition of furfurylsubstituted homoallylamines to allylhalides, acryloyl chloride and maleic anhydride
Varlamov A.V., Boltukhina E.V., Zubkov F.I., Nikitina E.V., Turchin K.F.
are formed via an initial amide formation followed by a stereoselective exo-IMDAF (Intramolecular Diels-Alder
Domino Wittig-Diels Alder reaction: Synthesis of carbazole lignans
Tilve S.G., Torney P.S., Patre R.E., Kamat D.P., Srinivasan B.R., Zubkov F.I.
reaction/Diels Alder reaction followed by aromatization with DDQ is described. The main step
First example of the cascade acylation/IMDAV/ene reaction sequence, leading to N-arylbenzo[f]isoindole-4-carboxylic acids possessing anti-viral activity
Voronov A.A., Alekseeva K.A., Ryzhkova E.A., Zarubaev V.V., Galochkina A.V., Zaytsev V.P., Majik M.S., Tilve S.G., Gurbanov A.V., Zubkov F.I.
anhydride, intramolecular Diels-Alder reaction of the vinylarene in the intermediate N-maleamide, and Alder
An IMDAF approach to annellated 1,4:5,8-diepoxynaphthalenes and their metathesis reaction leading to novel scaffolds displaying an antiproliferative activity toward cancer cells
Kvyatkovskaya E.A., Borisova K.K., Epifanova P.P., Senin A.A., Khrustalev V.N., Grigoriev M.S., Bunev A.S., Gasanov R.E., Polyanskii K.B., Zubkov F.I.
, was obtained via the intramolecular Diels-Alder furan (IMDAF) cycloaddition approach from bis-furyl dienes
Energy and volume activation parameters of the retro-Diels-Alder reaction in different solvents
Kiselev V., Kashaeva E., Bolotov A., Shakirova I., Konovalov A.
-chloroanthracene and tetracyanoethene by a Diels-Alder reaction were studied. The rate constants (298.2 K
Dramatic solvent effect on the volume of the Diels-Alder reaction between tetracyanoethylene and cyclopentadiene
Kiselev V., Kashaeva E., Shihab M., Medvedeva M., Konovalov A.
, cyclopentadiene, and their Diels-Alder adduct were determined at 25 °C. Eleven solvents of the π and n-donor type
Synthesis of benzothiazine sulfonamides via heteroatomic Diels-Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
Veremeichik Y., Shurpik D., Lodochnikova O., Plemenkov V.
and norbornadiene has afforded the Diels-Alder adducts of benzothiazine structure that have been oxidized
Hydrophobic acceleration in the Diels—Alder reaction of 9-hydroxymethylanthracene with N-phenylmaleimide
Kiselev V., Kashaeva H., Potapova L., Kornilov D., Latypova L., Konovalov A.
© 2016, Springer Science+Business Media New York.The Diels—Alder reaction rates of 9

Страница 7 из 1346

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