182284-86-2

Upstream product

• 182284-78-2 (R)-5-Butyl-5-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-dihydro-furan-2-one 
• 182284-79-3 (R)-4-((S)-1,2-Dihydroxy-ethyl)-4-hydroxy-octanoic acid methoxy-methyl-amide 
• 182284-94-2 (E)-(4S,5R)-5-(tert-Butyl-diphenyl-silanyloxy)-7-(4-methoxy-benzyloxy)-4-methyl-hept-2-enoic acid methyl ester 
• 182284-85-1 tert-Butyl-{(1R,2S)-4,4-dibromo-1-[2-(4-methoxy-benzyloxy)-ethyl]-2-methyl-but-3-enyloxy}-diphenyl-silane 
• 182284-84-0 (2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-5-(4-methoxy-benzyloxy)-2-methyl-pentanal 
• 182284-82-8 (Z)-3-{(2R,3R)-3-[2-(4-Methoxy-benzyloxy)-ethyl]-2-methyl-oxiranyl}-acrylic acid methyl ester 
• 182284-80-6 (R)-4-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-methylsulfanylmethoxy-octanoic acid methoxy-methyl-amide 
• 182284-83-9 (E)-(4S,5R)-5-Hydroxy-7-(4-methoxy-benzyloxy)-4-methyl-hept-2-enoic acid methyl ester 
• 182284-76-0 {(2S,3S)-3-Butyl-3-[3-(tetrahydro-pyran-2-yloxy)-propyl]-oxiranyl}-methanol 
• 182284-77-1 (S)-4-((R)-2-Butyl-tetrahydro-furan-2-yl)-2,2-dimethyl-[1,3]dioxolane 
• 5390-04-5 pent-1-yn-5-ol 
• 66084-35-3 6-tetrahydropyranyloxy-2-hexyn-1-ol 
• 62992-46-5 1-(tetrahydropyranyloxy)-4-pentyn 

Downstream Products

• 182284-87-3 tert-Butyl-{(1R,2S)-4-((1S,2R,5S)-2-butyl-2-methylsulfanylmethoxy-6,8-dioxa-bicyclo[3.2.1]oct-5-yl)-1-[2-(4-methoxy-benzyloxy)-ethyl]-2-methyl-butoxy}-diphenyl-silane 
• 182284-88-4 (3R,4S)-6-((1S,2R,5S)-2-Butyl-2-methylsulfanylmethoxy-6,8-dioxa-bicyclo[3.2.1]oct-5-yl)-1-(4-methoxy-benzyloxy)-4-methyl-hexan-3-ol 
• 182284-89-5 {(2S,3R,6S,8R,9S)-3-Butyl-8-[2-(4-methoxy-benzyloxy)-ethyl]-9-methyl-3-methylsulfanylmethoxy-1,7-dioxa-spiro[5.5]undec-2-yl}-methanol 
• 250379-11-4 (S)-1-{(2R,5S,7R,8S)-2-Butyl-7-[2-(4-methoxy-benzyloxy)-ethyl]-8-methyl-1,6-dioxa-spiro[4.5]dec-2-yl}-ethane-1,2-diol 

Relevant academic research and scientific papers

Synthetic studies on reveromycin A: Stereoselective synthesis of the spiroketal system

The 6,6-spiroketal system of reveromycin A (1), corresponding to the C9-C20 part, was stereoselectively synthesized and the absolute configuration at C11, C12, C15, C18 and C19 o