Abstract
A chiral rhodium(I)-diene catalyst enabled the one-step synthesis of β-aryl β-imido sulfones under mild reaction conditions. By selection of the chiral diene ligand L1a or L2, each enantiomer of the chiral β-aryl β-imido sulfone target can be accessed with high stereoselectivity. Demonstration of the scope of the reaction, which includes the synthesis of an N-protected chiral β-amino β-phenyl sulfone, culminated with the efficient synthesis of the heteroatom-rich active pharmaceutical ingredient apremilast.
Original language | English |
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Pages (from-to) | 4614-4618 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 21 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2019 Jun 21 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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CCDC 1907355: Experimental Crystal Structure Determination
Wu, H. (Contributor), Unknown Publisher, 2019
DOI: 10.5517/ccdc.csd.cc220rlg, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc220rlg&sid=DataCite
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