96735-59-0

Upstream product

• 56816-01-4 ethyl (S)-3-hydroxybutyrate 
• 83948-28-1 N-(trimethylsilyl)cinnamaldimine 
• 96735-59-0 (S)-3-((S)-1-Hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one 
• 96735-60-3 Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester 

Downstream Products

• 96735-60-3 Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester 
• 96735-59-0 (S)-3-((R)-1-Hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one 
• 96735-61-4 (S)-1-(tert-Butyl-dimethyl-silanyl)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-((E)-styryl)-azetidin-2-one 

Relevant academic research and scientific papers

AN ENANTIOSELECTIVE APPROACH TO CARBAPENEM ANTIBIOTICS: FORMAL SYNTHESIS OF (+)-THIENAMYCIN

An enantioselective synthesis of intermediates in synthesis of thienamycin (15) and epithienamycin-C (16) is described.

Stereocontrolled total synthesis of the chiral building block (3S,4R)-3-[(R)-1-hydroxyethyl]-4-acetyloxy-azetidin-2-one: A useful synthon for the synthesis of (+)-thienamycin, carbapenems and penems

A total stereocontrolled synthesis of (1), an intermediate in the synthesis of (+)-thienamycin, carbapenems and penems, based on a strategy that uses the S(-)hydroxyethylbutyrate as chiral building block, is reported.