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DBU-Catalyzed Alkyne-Imidate Cyclization toward 1-Alkoxypyrazino[1,2- a]indole Synthesis
Festa A.A., Zalte R.R., Golantsov N.E., Varlamov A.V., Voskressensky L.G., Van Der Eycken E.V.
, primary and secondary alcohols, and a thiol. The initial mechanistic study shows that the domino process
A Gold-Catalyzed Domino Cyclization Enabling Rapid Construction of Diverse Polyheterocyclic Frameworks
He Y., Li Z., Robeyns K., Van Meervelt L., Van Der Eycken E.V.
We report herein an efficient gold(I)-catalyzed post-Ugi domino dearomatization/ipso-cyclization
Synthesis of polycyclic imidazo[1,4]thiazine derivatives by an ANRORC domino reaction
Voskressensky L.G., Festa A.A., Sokolova E.A., Khrustalev V.N., Varlamov A.V.
that the domino sequence includes Kröhnke condensation, nucleophilic cyclization, and ANRORC (addition
Mn-Mediated sequential three-component domino Knoevenagel/cyclization/Michael addition/oxidative cyclization reaction towards annulated imidazo[1,2-a]pyridines
Sokolova E.A., Festa A.A., Storozhenko O.A.
Mn-Mediated sequential three-component domino Knoevenagel/cyclization/Michael addition
Alcohol-Initiated Dinitrile Cyclization in Basic Media: A Route Toward Pyrazino[1,2- a ]indole-3-Amines
Festa A.A., Golantsov N.E., Storozhenko O.A., Shumsky A.N., Varlamov A.V., Voskressensky L.G.
-initiated dinitrile cyclization, starting from N -(cyanomethyl)indole-2-carbonitriles under basic conditions
Mn-mediated sequential three-component domino Knoevenagel/cyclization/Michael addition/oxidative cyclization reaction towards annulated imidazo[1,2-a]pyridines
Storozhenko O.A., Festa A.A., Ndoutoume D.R.B., Aksenov A.V., Varlamov A.V., Voskressensky L.G.
and diethyl malonate. The formation of the target compounds presumably proceeds through a domino Knoevenagel/cyclization
Palladium-Catalyzed Domino Synthesis of 2,3-Difunctionalized Indoles via Migratory Insertion of Isocyanides in Batch and Continuous Flow
Chen S., Oliva M., Sharma U.K., Van Meervelt L., Van Der Eycken E.V.
Palladium-Catalyzed Domino Synthesis of 2,3-Difunctionalized Indoles via Migratory Insertion
A novel domino condensation-intramolecular nucleophilic cyclization approach towards annulated thiochromenes
Voskressensky L.G., Sokolova E.A., Festa A.A., Varlamov A.V.
,1-a]isoquinoline via a domino reaction of isoquinoline-derived iminium salts and α
A novel domino condensation - Intramolecular nucleophilic cyclization approach toward annulated imidazo-pyrrolopyridines
Voskressensky L.G., Storozhenko O.A., Festa A.A., Khrustalev V.N., Dang T.T.A., Nguyen V.T., Varlamov A.V.
]pyridine core proceeding through a base-promoted domino reaction of 6-azaindole quaternary salts, has been
Assembly of 1,2,3,4-Tetrahydropyrrolo[1,2- a]pyrazines via the Domino Reaction of 2-Imidazolines and Terminal Electron-Deficient Alkynes
Golantsov N.E., Golubenkova A.S., Festa A.A., Varlamov A.V., Voskressensky L.G.
then undergo a base-catalyzed domino aza-Claisen rearrangement/cyclization reaction sequence, simultaneously

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