2-环己基-2-氧代乙酸置于[ruthenium(II)(η6-1-Methyl-4-Isopropyl-Benzene)(Chloride)(μ-Chloride)]2 甲烷磺酸,(R)-(-)-[(S)-2-(Diphenylphosphino)Ferrocenyl]Ethyldi-Tert-Butylphosphine,氢气,三乙胺体系中,用 乙醇,1,2-二氯乙烷,甲苯 作为反应溶剂,25.0 °C,620.53 Kpa 条件下,反应 26.0H,反应生成 Cbz-环己基-L-甘氨酸
参考文献:Asymmetric Hydrogenation Of N-Sulfonylated-α-Dehydroamino Acids: Toward The Synthesis Of An Anthrax Lethal Factor Inhibitor
标题:Asymmetric Hydrogenation Of N-Sulfonylated-α-Dehydroamino Acids: Toward The Synthesis Of An Anthrax Lethal Factor Inhibitor
摘要:[graphic]A Novel And Highly Enantioselective Ru-Catalyzed Hydrogenation Of N-Sulfonylated-Alpha-Dehydroamino Acids Has Been Discovered And Demonstrated In The Synthesis Of An Anthrax Lethal Factor Inhibitor (Lfi). Herein,This Methodology Is Used To Prepare N-Sulfonylated Amino Acids In Up To 98% Ee. This Unprecedented Hydrogenation Uses A Chiral Ru Catalyst Rather Than Rh As Typical For Acylated Dehydroamino Acids And Esters,And This Work Reports The First Asymmetric Hydrogenation Of A Tetrasubstituted Dehydroamino Acid Derivative Using A Ru Catalyst.
DOI:10.1021/ol050869S