64468-56-0

Upstream product

• 1624-46-0 (E)-1,N-bis(4-methoxyphenyl)methanimine 
• 131533-40-9 1,4-bis(4-methoxyphenyl)azetidine-2,3-dione 
• 83306-67-6 p-methoxyphenylcarboxaldehyde N-(p-methoxyphenyl)imine 
• 41625-51-8 trimethylsiloxyacetic acid 

Relevant academic research and scientific papers

A novel asymmetric synthesis of 3-(1H-pyrrol-1-yl)-substituted β-lactams via a bismuth nitrate-catalyzed reaction

The reaction of racemic α-keto β-lactams 5a-5c with the commercially available chiral compound trans-4-hydroxy-L-proline (6) in the presence of a catalytic amount of Bi(NO3)3·5 H 2O in EtOH gave a diastereoisomer mixture o

Stereoselective synthesis of 3-alkylidene/alkylazetidin-2-ones from azetidin-2,3-diones

Azetidin-2,3-diones have been used as synthons for the synthesis of C-3 alkylidene/alkylazetidin-2-ones. Some of the 3-alkylazetidin-2-ones are well known for their cholesterol absorption inhibitor activity. A regio and stereoselective Grignard reaction o

Azetidin-2,3-dione synthon for stereoselective synthesis of cis- and trans-C-3-alkyl/aryl azetidin-2-ones

1,4-Bis-(4-methoxyphenyl)azetidin-2,3-dione has been prepared and used as a synthon for the stereoselective synthesis of C-3-alkyl/aryl azetidin-2-ones. Some of these are well known for their cholesterol absorption inhibitor activity. A regioselective Gri

Addition of α-bromoesters to Azetidine-2,3-diones Promoted by Zinc-Trimethylchlorosilane: A General Synthesis of 3-trimethylsilyloxyazetidin-2-ones and α-Alkylidene β-lactams.

A convenient procedure for the preparation of α-alkylidene β-lactams from monocyclic azetidine-2,3-diones by means of the Reformatsky reaction is described.

STEREOSELECTIVE ANNELATION OF TRIMETHYLSILOXYACETIC ACIDS AND IMINES INTO 3-HYDROXY-β-LACTAMS

Stereoselective synthesis of variously substituted 3-hydroxy-β-lactams can be achieved by the annelation of Schiff bases with trimethylsiloxyacetic acids promoted by phenyl dichlorophosphate reagent.A potential synthesis of N-unsubstituted β-lactams is ma