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An efficient synthesis of isoindolo[2,1-a]quinoline derivatives via imino Diels-Alder and intramolecular Diels-Alder reactions with furan
Kouznetsov V.V., Cruz U.M., Zubkov F.I., Nikitina E.V.
,2,3,4-tetrahydroquinolines bearing a furan fragment via the intramolecular Diels-Alder reaction is reported. The synthesis
Anomalies in the change of volumetric parameters of the Diels-Alder reaction in solution
Kiselev V., Bolotov A., Shakirova I., Kashaeva H., Potapova L., Konovalov A.
In this article negative values of the activation volume in retro-Diels-Alder reactions
Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One-Pot Approach to Arene-Fused Isoindolinones
Huang J., Du X., Pereshivko O.P., Peshkov V.A., Van Hecke K., Van Der Eycken E.V.
A one-pot procedure involving a four-component Ugi reaction followed by an intramolecular Diels–Alder
Anomalies in the change of volumetric parameters of the Diels-Alder reaction in solution
Kiselev V., Bolotov A., Shakirova I., Kashaeva H., Potapova L., Konovalov A.
In this article negative values of the activation volume in retro-Diels-Alder reactions
Cascade of the acylation/intramolecular oxo-Diels–Alder reaction for the diastereoselective synthesis of thienyl substituted hexahydropyrano[3,4-c]pyrrole-1,6-diones
Zaytsev V.P., Surina N.S., Pokazeev K.M., Shelukho E.R., Yakovleva E.D., Nadirova M.A., Novikov R.A., Khrustalev V.N., Zubkov F.I.
oxo-Diels–Alder reaction (IMODA), which is accompanied by the tautomerization step, and ends
The first example of an intramolecular Diels-Alder furan (IMDAF) reaction of iminium salts and its application in a short and simple synthesis of the isoindolo[1, 2-a]isoquinoline core of the jamtine and hirsutine alkaloids
Zubkov F.I., Ershova J.D., Zaytsev V.P., Obushak M.D., Matiychuk V.S., Sokolova E.A., Khrustalev V.N., Varlamov A.V.
-furyl-3, 4- dihydroisoquinolinium salt formation and subsequent intramolecular exo-Diels-Alder reaction
I ntra M olecular D iels- A lder Reactions of v inylarenes and Alkynyl Arenes (the IMDAV Reaction)
Krishna G., Grudinin D.G., Nikitina E.V., Zubkov F.I.
.3 Alkynes as Internal Dienophiles in Aryl Acetylenes (the Intramolecular Dehydro Diels-Alder Reaction) 8
An Intramolecular Diels-Alder Furan (IMDAF) Approach towards the Synthesis of Isoindolo[2,1- a ]quinazolines and Isoindolo[1,2- b ]quinazolines
Zaytsev V.P., Revutskaya E.L., Nikanorova T.V., Nikitina E.V., Dorovatovskii P.V., Khrustalev V.N., Yagafarov N.Z., Zubkov F.I., Varlamov A.V.
Diels-Alder furan (IMDAF) reaction of 2-furylquinazolinones is described. Reactions of α
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.
-oxatricyclo[5.2.1.0(1,5)]dec-8-ene-6-carboxylic acid via amide formation followed by intramolecular Diels-Alder
The intramolecular Diels-Alder vinylfuran (IMDAV) reaction: a short approach to aza-analogues of pinguisane-type sesquiterpenes
Horak Y.I., Lytvyn R.Z., Homza Y.V., Zaytsev V.P., Mertsalov D.F., Babkina M.N., Nikitina E.V., Lis T., Kinzhybalo V., Matiychuk V.S., Zubkov F.I., Varlamov A.V., Obushak M.D.
[2,3-f]isoindoles - the aza-analogs of pinguisane-type sesquiterpenes. The key intramolecular Diels-Alder

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