189079-64-9

Upstream product

• 189079-67-2 (3R,4S,5R)-4-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-5-phenyl-pentanethioic acid S-tert-butyl ester 
• 1053263-28-7 (3R,4S,5R)-4-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-3-trimethylsilanyloxy-pentanethioic acid S-tert-butyl ester 
• 1053634-71-1 (3R,4S,5R)-4-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-3-trimethylsilanyloxy-pentan-1-ol 
• 1054653-00-7 Benzoic acid (R)-{(4S,5R)-5-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-phenyl-methyl ester 
• 189079-63-8 (2S,3R,1'R)-2-(1'-benzoyloxy-1'-phenylmethyl)-3-hydroxy-5-methoxytetrahydrofuran 
• 189079-59-2 (1R,2S,3R)-2-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-1-phenyl-pentane-1,3-diol 
• 189079-62-7 (1R,2S,3R)-1-benzoyloxy-5-hydroxy-2,3-isopropylidenedioxy-1-phenylpentane 
• 189079-61-6 (R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-((4S,5R)-2,2-dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-propan-1-ol 
• 189079-60-5 (R)-{(4R,5R)-5-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-phenyl-methanol 
• 1053734-98-7 (1R,2S,3R)-2-Benzyloxy-1-phenyl-pentane-1,3,5-triol 
• 98-88-4 benzoyl chloride 

Relevant academic research and scientific papers

New approach to AI-77B: Stereoselective construction of a potential precursor of the amino acid side chain

A potential precursor of the amino acid side-chain derivative of antiulcerogenic antibiotic AI-77B is prepared in a highly stereoselective manner from the anti-aldol product 3, obtained from the reaction of the chiral benzaldehydechromium(0) complex 2.