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 Gonzalezsubject
Cascade reactionAmino estersChemistryStereochemistryDiastereomerAza-Diels–Alder reactionStereoselectivityGeneral MedicineHydroaminationStereocenterCatalysisdescription
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.
year | journal | country | edition | language |
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2013-06-03 | ChemInform |