Metal-Free Synthesis of Functionalized Tetrasubstituted Alkenes by Three-Component Reaction of Alkynes, Iodine, and Sodium Sulfinates. [PDF]
Zhang J +5 more
europepmc +1 more source
Copper-Catalyzed 1,2-Amino Oxygenation of 1,3-Dienes: A Chemo-, Regio-, and Site-Selective Three-Component Reaction with O-Acylhydroxylamines and Carboxylic Acids. [PDF]
Hemric BN, Chen AW, Wang Q.
europepmc +1 more source
The LANCA three-component reaction to highly substituted β-ketoenamides - versatile intermediates for the synthesis of functionalized pyridine, pyrimidine, oxazole and quinoxaline derivatives. [PDF]
Lechel T +4 more
europepmc +1 more source
A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: a mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates. [PDF]
Németh AG +2 more
europepmc +1 more source
Development of Novel and Efficient Processes for the Synthesis of 5-Amino and 5-Iminoimidazo[1,2-a]imidazoles via Three-Component Reaction Catalyzed by Zirconium(IV) Chloride. [PDF]
Driowya M +3 more
europepmc +1 more source
Synthesis of a novel category of pseudo-peptides using an Ugi three-component reaction of levulinic acid as bifunctional substrate, amines, and amino acid-based isocyanides. [PDF]
Khalesi M +2 more
europepmc +1 more source
An efficient and ecofriendly synthesis of highly functionalized pyridones via a one-pot three-component reaction. [PDF]
Hosseini H, Bayat M.
europepmc +1 more source
Regioselectivity and diastereoselectivity of three-component reaction of α-amino acid, dialkyl acetylenedicarboxylates and 2-arylidene-1,3-indanediones. [PDF]
Chen L, Sun J, Huang Y, Zhang Y, Yan CG.
europepmc +1 more source
Formation of diverse polycyclic spirooxindoles via three-component reaction of isoquinolinium salts, isatins and malononitrile. [PDF]
Sun J, Shen GL, Huang Y, Yan CG.
europepmc +1 more source
One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction. [PDF]
Yang B, Tao C, Shao T, Gong J, Che C.
europepmc +1 more source

