182284-89-5

Upstream product

• 1054709-81-7 (R)-4-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-triethylsilanyloxy-ethyl]-4-methylsulfanylmethoxy-octanoic acid methoxy-methyl-amide 
• 250378-97-3 (S)-1-((R)-2-Butyl-tetrahydro-furan-2-yl)-ethane-1,2-diol 
• 849619-01-8 1-(4-methoxybenzyloxy)-4-methylhex-5-en-3-ol 
• 66084-35-3 6-tetrahydropyranyloxy-2-hexyn-1-ol 
• 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 
• 182284-86-2 (3R,4S,10R)-3-(tert-Butyl-diphenyl-silanyloxy)-10-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-(4-methoxy-benzyloxy)-4-methyl-10-methylsulfanylmethoxy-tetradecan-7-one 
• 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 
• 182284-80-6 (R)-4-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-methylsulfanylmethoxy-octanoic acid methoxy-methyl-amide 
• 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 
• 62992-46-5 1-(tetrahydropyranyloxy)-4-pentyn 
• 250379-08-9 Triethyl-{(1R,2S)-1-[2-(4-methoxy-benzyloxy)-ethyl]-2-methyl-but-3-ynyloxy}-silane 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 

Relevant academic research and scientific papers

Total synthesis of reveromycin A

matrix presented The stereoselective total synthesis of reveromycin A (1), a potent inhibitor of eukaryotic cell growth, has been accomplished on the basis of the stereocontrolled construction of the 6,6-spiroketal system, efficient succinylation of the t

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