jo7b01927_si_002.cif (444.46 kB)
Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Hydroamination Sequence: Expeditious Access to Enantioenriched Pyrroloisoquinoline Derivatives
dataset
posted on 2017-09-21, 00:00 authored by Alba Molina, Ana Pascual-Escudero, Javier Adrio, Juan C. CarreteroA three-step
reaction sequence has been developed to prepare a
variety of enantioenriched pyrroloisoquinoline derivatives. The process
involves a catalytic asymmetric azomethine ylide 1,3-dipolar cycloaddition
followed by an intramolecular AuI-catalyzed alkyne hydroamination
and enamine reduction.