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Thiourea fused γ-amino alcohol organocatalysts for asymmetric Mannich reaction of β-keto active methylene compounds with imines†
Miku Nomura,Zubeda Begum,Chigusa Seki,Eunsang Kwon,Koji Uwai,Michio Tokiwa,Suguru Tokiwa,Mitsuhiro Takeshita,Hiroto Nakano
RSC Advances Pub Date : 01/26/2023 00:00:00 , DOI:10.1039/D2RA08317E
Abstract

Catalytic functionality of new optically active thiourea fused γ-amino alcohols was examined in the asymmetric Mannich reaction of β-keto active methylene compounds with imines to afford chiral Mannich products, β-amino keto compounds, with continuous chiral centers, that are versatile synthetic intermediates for deriving various biologically active compounds. In particular, the thiourea fused γ-amino alcohols showed satisfactory catalytic activity in this reaction and afforded chiral Mannich products in excellent chemical yield (up to 88%) and stereoselectivities (up to syn : anti/93 : 7 dr, up to 99% ee).

Graphical abstract: Thiourea fused γ-amino alcohol organocatalysts for asymmetric Mannich reaction of β-keto active methylene compounds with imines
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