147461-21-0

Upstream product

• 131722-62-8 1,2:5,6-dianhydro-3,4-dideoxy-erythro-hexitol 
• 147461-20-9 (S)-(R)-4-Oxiranyl-butan-2-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 147461-24-3 (E)-(4R,7S)-7-(tert-Butyl-diphenyl-silanyloxy)-4-hydroxy-oct-2-enoic acid methyl ester 
• 147461-31-2 (E)-(4S,7S)-7-(tert-Butyl-diphenyl-silanyloxy)-4-hydroxy-oct-2-enoic acid methyl ester 
• 147461-26-5 (E)-3-{2-[(S)-3-(tert-Butyl-diphenyl-silanyloxy)-butyl]-[1,3]dioxolan-2-yl}-acrylic acid methyl ester 
• 147461-28-7 (4R,7S)-7-(tert-Butyl-diphenyl-silanyloxy)-4-methanesulfonyloxy-octanoic acid 
• 147461-25-4 (E)-(S)-7-(tert-Butyl-diphenyl-silanyloxy)-4-oxo-oct-2-enoic acid methyl ester 
• 147461-29-8 (S)-5-[(S)-3-(tert-Butyl-diphenyl-silanyloxy)-butyl]-dihydro-furan-2-one 
• 147461-27-6 (5S,8S)-8-(tert-Butyl-diphenyl-silanyloxy)-non-1-en-5-ol 

Relevant academic research and scientific papers

Preparation of macrodiolides via a common chiral building block. Total synthesis of (-)-pyrenophorin and (-)-pyrenophorol

Macrodiolides (-)-pyrenophorin and (-)-pyrenophorol have been synthesized utilizing a C2 symmetric (R,R)-diepoxide as a common enantiopure chiral building block.