Post-Ugi cyclization for the construction of diverse heterocyclic compounds: Recent updates the door for desired
post-Ugi modifications. In recent times, the
post-Ugi transformation has proved
Gold-catalyzed post-MCR transformations towards complex (poly)heterocycles affords a linear peptide backbone, enabling
post-Ugi transformations as an elegant solution to rigidify
Recent Advances in the Synthesis of Peptidomimetics via Ugi Reactions by
post-Ugi transformations. Organo-catalyzed reactions, base-promoted reactions, and metal-free reactions
Recent advances in post Ugi-4CR dearomatizations for constructing spiro heterocycles. The
Ugi adducts provide myriad opportunities for
post-transformations, leading to heterocycles, bioactive
Divergent Access to Imidazopyrazinones and Imidazodiazepinones by Regioswitchable Post-Ugi Heteroannulation-component reaction of easily available building blocks and an exo/endo selectivity-switchable
post-Ugi intramolecular
Microwave-Assisted Post-Ugi Reactions for the Synthesis of PolycyclesMicrowave-Assisted
Post-Ugi Reactions for the Synthesis of Polycycles
Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolonesA series of propargylamides containing an electron-rich benzene ring was prepared through the
Ugi Sulfur modification in natural RNA and therapeutic oligonucleotidesIn this review, we highlight the importance of sulfur
modifications in natural cellular RNAs
Post‐Ugi Cyclizations Towards Polycyclic N‐Heterocycles. By carefully selecting the starting four components,
Ugi‐adducts could undergo different kinds of
post