Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Aryl Allyl Phthalimides.

Org Lett

Institute for Research in Biomedicine (IRB Barcelona) , The Barcelona Institute of Science and Technology (BIST), Baldiri Reixac 10 , 08028 Barcelona , Spain.

Published: December 2019

The iridium-catalyzed asymmetric hydrogenation of 2-aryl allyl phthalimides to afford enantioenriched β-aryl-β-methyl amines is presented. Recently developed Ir-MaxPHOX catalysts are used for this enantioselective transformation. The mild reaction conditions and the feasible removal of the phthalimido group makes this catalytic method easily scalable and of great interest to afford chiral amines. The importance of this new methodology is exemplified by the formal synthesis of ()-Lorcaserin, OTS514, and enantiomerically enriched 3-methyl indolines.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.9b03865DOI Listing

Publication Analysis

Top Keywords

hydrogenation 2-aryl
8
2-aryl allyl
8
allyl phthalimides
8
highly enantioselective
4
enantioselective iridium-catalyzed
4
iridium-catalyzed hydrogenation
4
phthalimides iridium-catalyzed
4
iridium-catalyzed asymmetric
4
asymmetric hydrogenation
4
phthalimides afford
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!