594855-18-2

Upstream product

• 18107-18-1 diazomethyl-trimethyl-silane 
• 487-68-3 mesytaldehyde 
• 594855-17-1 (2R,4S)-4-((Z)-(S)-5-{3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-chloro-4-methyl-pent-2-enyl)-2-(2,4,6-trimethyl-phenyl)-[1,3]dioxolane-4-carboxylic acid methyl ester 
• 594854-60-1 dithiocarbonic acid O-(3-(tert-butyl-dimethyl-silanyloxy)-1-{3-[1-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-methyl-propyl) ester S-methyl ester 
• 594854-59-8 3-(tert-butyl-dimethyl-silanyloxy)-1-{3-[1-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-methyl-propan-1-ol 
• 594854-58-7 3-(tert-butyl-dimethyl-silanyloxy)-1-{3-[1-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-methyl-propan-1-one 
• 594854-61-2 1-[3-(tert-butyl-dimethyl-silanyloxy)-2-methyl-propyl]-3-[1-(tert-butyl-dimethyl-silanyloxy)-propyl]-benzene 
• 594855-14-8 (Z)-(S)-5-{3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-chloro-4-methyl-pent-2-enoic acid ethyl ester 
• 594855-16-0 tert-Butyl-{(S)-1-[3-((Z)-(S)-4-chloro-5-iodo-2-methyl-pent-3-enyl)-phenyl]-propoxy}-dimethyl-silane 
• 594855-15-9 (Z)-(S)-5-{3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-chloro-4-methyl-pent-2-en-1-ol 
• 594854-57-6 (R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-[3-((S)-1-hydroxy-propyl)-phenyl]-2-methyl-propan-1-one 
• 594854-62-3 (S)-3-{3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-methyl-propan-1-ol 
• 594855-02-4 (S)-3-{3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-phenyl}-2-methyl-propionaldehyde 
• 224622-38-2 (S)-1-(3'-bromophenyl)-1-propanol 

Downstream Products

• 594855-19-3 (2R,4S)-4-{(Z)-(S)-5-[3-((S)-1-Acetoxy-propyl)-phenyl]-2-chloro-4-methyl-pent-2-enyl}-2-(2,4,6-trimethyl-phenyl)-[1,3]dioxolane-4-carboxylic acid methyl ester 
• 594855-21-7 C₃₁H₃₇ClO₅ 
• 594855-22-8 C₃₁H₃₇ClO₅ 
• 594855-20-6 C₃₀H₃₅ClO₅ 

Relevant academic research and scientific papers

Synthesis and antifungal activity of novel 14-membered benzomacrolides, as galbonolide analogues

Asymmetric total synthesis of benzene analogues of galbonolide, a 14-membered antifungal macrolide, possessing a benzene ring instead of a conjugated diene structure, was achieved starting from chiral 1-aryl-1-propanol obtained by enzyme-catalyzed kinetic