872693-82-8

Upstream product

• 149401-42-3 (E)-5-(benzyloxy)pent-3-en-2-one 
• 503004-69-1 (1S,4R,2E)-acrylic acid 1-allyl-4-methoxymethoxy-4-methyl-5-triisopropylsilyloxypent-2-enyl ester 
• 503004-60-2 (2R,3E)-(5-benzyloxy-2-methoxymethoxy-2-methyl-pent-3-enyloxy)triisopropylsilane 
• 503004-62-4 (3'R,6R,1'E)-6-(3'-methoxymethoxy-3'-methyl-4'-triisopropylsilyloxybut-1'-enyl)-5,6-dihydro-pyran-2-one 
• 503004-67-9 (2R,3E)-5-benzyloxy-2-methyl-1-triisopropylsilyloxypent-3-en-2-ol 
• 503004-68-0 (4R,2E)-4-methoxymethoxy-4-methyl-5-triisopropylsilyloxy-pent-2-en-1-ol 
• 503004-57-7 (2R,3E)-5-benzyloxy-2-methyl-2-trimethylsilyloxypent-3-enenitrile 
• 503004-56-6 (4R,2E)-4-methoxymethoxy-4-methyl-5-triisopropylsilyloxypent-2-enal 
• 503004-70-4 (3'R,6R,1'E)-6-(4'-hydroxy-3'-methoxymethoxy-3'-methylbut-1'-enyl)-5,6-dihydro-pyran-2-one 
• 503004-58-8 (2R,3E)-5-benzyloxy-2-methyl-pent-3-ene-1,2-diol 
• 503004-55-5 (2R,2'R,3E)-2-methoxymethoxy-2-methyl-4-(6'-oxo-3',6'-dihydro-2H-pyran-2'-yl)but-3-enal 

Relevant academic research and scientific papers

Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin

Catalytic asymmetric synthesis of the natural antibiotic fostriecin (CI-920) and its analogue 8-epi-fostriecin and evaluation of their biological activity are described. We used four catalytic asymmetric reactions to construct all of the chiral centers of