Asymmetric Synthesis of β‑Aryl β‑Imido Sulfones Using Rhodium Catalysts with Chiral Diene Ligands: Synthesis of Apremilast

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 t...

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Veröffentlicht in:Organic letters 2019-06, Vol.21 (12), p.4614-4618
Hauptverfasser: Syu, Jin-Fong, Gopula, Balraj, Jian, Jia-Hong, Li, Wei-Sian, Kuo, Ting-Shen, Wu, Ping-Yu, Henschke, Julian P, Hsieh, Meng-Chi, Tsai, Ming-Kang, Wu, Hsyueh-Liang
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Sprache:eng
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Zusammenfassung: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.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b01513