924288-72-2

Upstream product

• 100-39-0 benzyl bromide 
• 1312103-67-5 C₃₃H₄₃IO₄Si 
• 1312103-57-3 ((4S,5S)-5-((R)-1-(benzyloxy)-4-((tert-butyldiphenylsilyl)oxy)butyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol 
• 1312103-54-0 (4R,5S)-5-((R)-1-(benzyloxy)-4-hydroxybutyl)-N-methoxy-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide 
• 1312103-53-9 (4R,5S)-5-((R)-1-(benzyloxy)pent-4-en-1-yl)-N-methoxy-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide 
• 1053694-92-0 (4R,5S)-5-((R)-1-hydroxypent-4-en-1-yl)-N-methoxy-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide 
• 1826-67-1 vinyl magnesium bromide 
• 924288-73-3 4,5-bis-[1-benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-2,2-dimethyl-[1,3]dioxolane 
• 924288-71-1 4,7-bis-benzyloxy-1,10-bis-(tert-butyl-diphenyl-silanyloxy)-decane-5,6-diol 
• 924288-70-0 4-benzyloxy-4-[5-(1-benzyloxy-4-hydroxy-butyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-butan-1-ol 
• 874910-07-3 (4S,5S)-4,5-bis((R)-1-(benzyloxy)pent-4-enyl)-2,2-dimethyl-1,3-dioxolane 
• 874910-06-2 (4S,5S)-4,5-bis((R)-1-hydroxypent-4-enyl)-2,2-dimethyl-1,3-dioxolane 
• 874910-05-1 (4R,5R)-4,5-bis(pent-4-enoyl)-2,2-dimethyl-1,3-dioxolane 

Downstream Products

• 852509-26-3 (5R,6R,7E,10S)-10-[(1'S)-1'-benzyloxyheptyl]-5,6-dibenzyloxy-3,4,5,6,9,10-hexahydro-2H-oxecin-2-one 
• 852509-25-2 (4R,5R)-4,5-dibenzyloxyhept-6-enoic acid (1'S,1''S)-1'-(1''-benzyloxyheptyl)-3'-butenyl ester 
• 553665-24-0 (4R,5R)-4,5-bis(benzyloxy)hept-6-en-1-ol 
• 553664-97-4 (4R,5R)-4,5-bis(benzyloxy)hept-6-enoic acid 
• 924288-74-4 (4,5-bis-benzyloxy-hept-6-enyloxy)-tert-butyl-diphenyl-silane 

Relevant academic research and scientific papers

Enantiodivergent total synthesis of microcarpalide from l-tartaric acid

Stereoselective approach for the synthesis of both enantiomers of bio-active decanolactone microcarpalide is described from l-tartaric acid. The synthesis of the key intermediates en route to the natural product is achieved from l-tartaric acid involving

Stereoselective synthesis of (-)-microcarpalide

A stereoselective approach for the synthesis of the bio-active decanolactone (-)-microcarpalide was achieved from chiral pool tartaric acid. The synthesis of pivotal intermediates en route to the decanolactone was achieved from α-benzyloxy aldehydes deriv