107148-95-8

Upstream product

• 951-82-6 3,4,5-trimethoxyphenyl acetic acid 
• 107148-84-5 (2R)-(-)-1-(triphenylmethoxy)-2-<(methylsulfonyl)oxy>propane 
• 107148-83-4 (2S)-(+)-1-(triphenylmethoxy)-2-<(methylsulfonyl)oxy>propane 

Downstream Products

• 107148-99-2 (2S,3S)-(-)-2-(2-propenyl)-2-(3,4,5-trimethoxyphenyl)-3-methylbutyrolactone 
• 107149-00-8 (2R,3R)-(+)-2-(2-propenyl)-2-(3,4,5-trimethoxyphenyl)-3-methylbutyrolactone 
• 38176-10-2 (+)-Gallopamil 
• 107149-09-7 (R)-N¹-[2-(3,4-Dimethoxy-phenyl)-ethyl]-4-isopropyl-N¹-methyl-4-(3,4,5-trimethoxy-phenyl)-pentane-1,5-diamine 
• 107173-91-1 (2R,3R)-(-)-1-<(methylsulfonyl)oxy>-2-methyl-3-cyano-3-(3,4,5-trimethoxyphenyl)hex-5-ene 
• 116759-58-1 Methanesulfonic acid (R)-4-cyano-5-methyl-4-(3,4,5-trimethoxy-phenyl)-hexyl ester 
• 107149-02-0 (2R,3R)-(-)-2-methyl-3-cyano-3-(3,4,5-trimethoxyphenyl)hex-5-enol 
• 107149-08-6 N-<(2S)-2-(3,4,5-trimethoxyphenyl)-2-isopropyl-5-<(3,4-dimethoxyphenethyl)methylamino>pentyl>-(1S)-10-camphorsulfonamide 

Relevant academic research and scientific papers

Diastereo- And Enantioselective Synthesis of Structurally Diverse Succinate, Butyrolactone, and Trifluoromethyl Derivatives by Iridium-Catalyzed Hydrogenation of Tetrasubstituted Olefins

A highly efficient iridium N,P-ligand-catalyzed asymmetric hydrogenation of functionalized tetrasubstituted olefins lacking a directing group has been developed. Various structural diverse chiral succinate derivatives were obtained in high yields and exce