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Highly efficient azido-Ugi multicomponent reactions for the synthesis of bioactive tetrazoles bearing sulfonamide scaffolds
Nazeri M.T., Nowee A.B., Javanbakht S., Farhid H., Shaabani A., Notash B.
is the formation of an intermediate Schiff base and its activation in the azido-Ugi reaction by a Lewis acid
New family of polydentate tetrazole-pyrazoline ligands prepared by the azido-Ugi reaction
Gorbacheva A.M., Krutov I.A., Vorozhtsov N.I., Khrustalev V.N., Nenajdenko V.G.
by the efficient azido-Ugi reaction of N-(arylidene)pyrazolinium salts with isocyanides and sodium azide in up
Efficient synthesis of tetrazole derivatives of cytisine using the azido-Ugi reaction
Zarezin D.P., Kabylda A.M., Vinogradova V.I., Dorovatovskii P.V., Khrustalev V.N., Nenajdenko V.G.
The azido-Ugi reaction with natural alkaloid cytisine was investigated. It was demonstrated
Functionalization of Poplar cotton via azido-Ugi reaction: as a green biocatalytic system for the chemical fixation of CO2
Nazeri M.T., Ghasemi M., Torabi S., Shaabani A.
periodate and participated in the azido-Ugi four-component reaction (AU-4CRs) of sulfonamide, isocyanide
Diastereoselectivity of Azido-Ugi Reaction with Secondary Amines. Stereoselective Synthesis of Tetrazole Derivatives
Zarezin D.P., Khrustalev V.N., Nenajdenko V.G.
The diastereoselectivity of azido-Ugi reaction with cyclic amines was investigated. It was found
Synthesis of 1-tetrazolyl substituted 1,2,3,4-tetrahydroisoquinolines via azido-Ugi reaction and investigation of their reactivity with activated alkynes
Samavati R., Aleksandrova E.V., Miftyakhova A.R., Titov А.А., Varlamov А.V.
Synthesis of 1-tetrazolyl substituted 1,2,3,4-tetrahydroisoquinolines via azido-Ugi reaction
Using Triazolobenzodiazepine as the Cyclic Imine in Various Types of Joullié–Ugi Reactions
Nazeri M.T., Ghasemi M., Ahmadi M., Shaabani A., Notash B.
of triazolobenzodiazepine in the Joullié-Ugi, azido-Joullié-Ugi, and pseudo-Joullié-Ugi reactions of a broad scope
A concise approach toward tetrazolyl-substituted benzazocines via a novel isocyanide-based multicomponent reaction
Borisov R.S., Voskressensky L.G., Polyakov A.I., Borisova T.N., Varlamov A.V.
sequential azido-Ugi and alkyne-induced ring-expansion reactions starting from cotarnine chloride
Post-Ugi cyclization for the construction of diverse heterocyclic compounds: Recent updates
Bariwal J., Kaur R., Voskressensky L.G., Van Der Eycken E.V.
and with high atom economy. One of the dominant MCRs is the Ugi reaction, which involves the condensation
Recent Advances in the Synthesis of Peptidomimetics via Ugi Reactions
Liu C., Voskressensky L.G., Van der Eycken E.V.
made to synthesize various peptidomimetics. Among them, the Ugi reaction is a popular way

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