919298-91-2

Upstream product

• 184528-64-1 (2S,3S)-3,4-(di(tert-butyldimethylsilyloxy))-2-methyl-butanal 
• 919298-90-1 5,6-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4-dimethyl-hexan-1-ol 
• 919298-80-9 4-[2,3-bis(tert-butyldimethylsilyloxy)-1-methyl-propyl]-2-(4-methoxyphenyl)-5-methyl-[1,3]dioxane 
• 919298-79-6 5,6-bis-(tert-butyl-dimethyl-silanyloxy)-2,4-dimethyl-hexane-1,3-diol 
• 919298-81-0 C₃₅H₆₀O₅Si₂ 

Downstream Products

• 919298-99-0 7,9,13,19-tetrakis-(tert-butyl-dimethyl-silanyloxy)-21-(4-methoxy-benzyloxy)-6,12,14,16,20,22-hexamethyl-hexacosa-2,4,10,23,25-pentaenoic acid ethyl ester 
• 919298-85-4 (2Z,4E,6R,7S,9S,10Z,12S,13R,14S,16S,19R,21S,22S,23Z)-9-hydroxy-21-(4-methoxy-benzyloxy)-7,13,19-tris(tert-butyldimethylsilyloxy)-6,12,14,16,20,22-hexamethyl-hexaeicosa-2,4,10,23,25-pentaenoic acid ethyl ester 
• 919298-82-1 C₅₁H₉₂O₆Si₃ 
• 919298-83-2 (+)-1-methoxy-4-[(1S,2R,3R,6S,8S,9R,10S)-3,9,11-tris-(tert-butyldimethylsilanyloxy)-2,6,8,10-tetramethyl-1-((Z)-(S)-1-methylpenta-2,4-dienyl)undecyloxymethyl]benzene 
• 919298-94-5 5,11,13-tris-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4,8,10,12-pentamethyl-tridecan-1-ol 
• 919298-93-4 2-(4-methoxy-phenyl)-5-methyl-4-[2,8,10-tris-(tert-butyl-dimethyl-silanyloxy)-1,5,7,9-tetramethyl-decyl]-[1,3]dioxane 
• 919298-95-6 5,11,13-tris-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4,8,10,12-pentamethyl-tridecanal 
• 919298-84-3 (5R,6S,8S,11R)-5-((S,Z)-4-iodobut-3-en-2-yl)-11-((2R,3S,4S,Z)-3-(4-methoxybenzyloxy)-4-methylocta-5,7-dien-2-yl)-2,2,3,3,6,8,13,13,14,14-decamethyl-4,12-dioxa-3,13-disilapentadecane 
• 919298-96-7 (+)-(Z)-(2S,3R,4S,6S,9R,10R,11S,12S)-3,9-bis-(tert-butyldimethylsilanyloxy)-11-(4-methoxybenzyloxy)-2,4,6,10,12-pentamethylhexadeca-13,15-dien-1-ol 
• 919298-97-8 (-)-(Z)-(2R,3R,4S,6S,9R,10R,11S,12S)-3,9-bis-(tert-butyldimethylsilanyloxy)-11-(4-methoxybenzyloxy)-2,4,6,10,12-pentamethylhexadeca-13,15-dienal 
• 919298-75-2 6-benzyloxy-2-(tert-butyldimethylsilyloxy)-4-(4-methoxybenzyloxy)-3,5-dimethylhexanal 

Relevant academic research and scientific papers

Total synthesis of potential antitumor agent, (-)-dictyostatin

(Chemical Equation Presented) The potential antitumor agent (-)-dictyostatin has been synthesized utilizing Brown crotylboration to achieve eight of the eleven chiral centers. The yield for the 26-step longest sequence is ～4%. The C9-C10 coupling is achie