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The first synthesis of 8,10a-epoxypyrido[2,1-a]iso-indolo-7-carboxylic acids
Zubkov F.I., Zaytsev V.P., Nikitina E.V., Borisov R.S., Airiyan I.K., Turchin K.F., Varlamov A.V.
Diels-Alder reaction
Novel approach to isoindolo[2,1-a]quinolines: Synthesis of 1- and 3-halo-substituted 11-oxo-5,6,6a,11-tetrahydroisoindolo[2,1-a]quinoline-10- carboxylic acids
Boltukhina E.V., Zubkov F.I., Nikitina E.V., Varlamov A.V.
Intramolecular Diels-Alder reactions
First representative of 6b,9-epoxyisoindolo-[2,1-a]quinazoline-10-carboxylic acids
Zaytsev V.P., Zubkov F.I., Motorygina E.L., Gorbacheva M.G., Nikitina E.V., Varlamov A.V.
Diels-Alder reaction
Novel approach to synthesis of [c]-condensed decahydroisoindolo[2,1-a]quinolines
Zubkov F.I., Zaytsev V.P., Nikitina E.V., Mikhaylova N.M., Aleksandrov G.G., Borisov R.S., Varlamov A.V.
Diels-Alder reaction
Preparative synthesis of 7-carboxy-2-R-isoindol-1-ones
Varlamov A.V., Boltukhina E.V., Zubkov F.I., Sidorenko N.V., Chernyshev A.I., Grudinin D.G.
Intramolecular Diels-Alder reaction
A general strategy for the synthesis of oxoisoindolo[2,1-a]quinoline derivatives: The first efficient synthesis of 5,6,6a,11-tetrahydro-11-oxoisoindolo[2,1-a]quinoline-10-carboxylic acids
Varlamov A.V., Zubkov F.I., Boltukhina E.V., Sidorenko N.V., Borisov R.S.
Intramolecular Diels-Alder reaction
A new approach to construction of isoindolo[1,2-a]isoquinoline alkaloids Nuevamine, Jamtine, and Hirsutine via IMDAF reaction
Zubkov F.I., Ershova J.D., Orlova A.A., Zaytsev V.P., Nikitina E.V., Peregudov A.S., Gurbanov A.V., Borisov R.S., Khrustalev V.N., Maharramov A.M., Varlamov A.V.
that the reaction proceeds via amide formation and subsequent intramolecular Diels-Alder reaction of the furan
The short route to chalcogenurea-substituted 3a,6-epoxyisoindoles via an intramolecular Diels-Alder furan (IMDAF) reaction. Antibacterial and antifungal activity
Mertsalov D.F., Shchevnikov D.M., Lovtsevich L.V., Novikov R.A., Khrustalev V.N., Grigoriev M.S., Romanycheva A.A., Shetnev A.A., Bychkova O.P., Trenin A.S., Zaytsev V.P.
consecutive steps: the nucleophilic addition reaction and the intramolecular Diels-Alder furane (IMDAF
A two-stage synthesis of 8,10a-epoxypyrido[2,1-a]isoindoles: Stereochemistry of the [4+2] cycloaddition of maleic anhydride with 2,6-difurylpiperidin-4-ones
Zubkov F.I., Airiyan I.K., Turchin K.F., Zaytsev V.P., Gurbanov A.V., Maharramov A.M., Khrustalev V.N., Peregudov A.S., Nikitina E.V., Varlamova A.V.
the intramolecular Diels-Alder reaction has been demonstrated. It has been shown that a one-stage synthesis
Iodine Acetate as a Mild Selective Agent for the Wagner–Meerwein Rearrangement in 3a,6-Epoxyisoindoles
Zaytsev V.P., Mertsalov D.F., Trunova A.M., Khanova A.V., Nikitina E.V., Sinelshchikova A.А., Grigoriev M.S.
of iodine acetate in acetic anhydride the reaction proceeds regio- and stereoselectively with the formation

Страница 3 из 1330

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