6533b7d0fe1ef96bd125a22c

RESEARCH PRODUCT

ChemInform Abstract: Gold Catalyzed Stereoselective Tandem Hydroamination-Formal Aza-Diels-Alder Reaction of Propargylic Amino Esters.

Carlos Del PozoSantos FusteroJavier MiróPaula BelloMaría Sánchez-rosellóMiguel A. MaestroJavier Gonzalez

subject

Cascade reactionAmino estersChemistryStereochemistryDiastereomerAza-Diels–Alder reactionStereoselectivityGeneral MedicineHydroaminationStereocenterCatalysis

description

The overall sequence of the tandem reaction presented here leads to nitrogen-containing tetracycles under formation of 4 bonds and five stereocenters, in most cases as single diastereoisomers.

https://doi.org/10.1002/chin.201325137