882005-07-4

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 882005-20-1 (2R,4R,6S)-7-Benzyloxy-2,4,6-trimethyl-heptanal 
• 333354-15-7 ((((2S,4S,6R)-2,4,6-trimethyloct-7-en-1-yl)oxy)methyl)benzene 
• 730964-33-7 (2S,4R,6R)-7-[1-(tert-butyl)-1,1-dimethylsilyl]oxy-2,4,6-trimethylheptan-1-ol 
• 730964-37-1 (4R,6R)-7-tert-butyldimethylsilyloxy-4,6-dimethyl-1-heptene 
• 730964-32-6 (R)-tert-butyldimethyl((2-methylpent-4-en-1-yl)oxy)silane 
• 174627-70-4 (2R,4S,6S)-7-(benzyloxy)-2,4,6-trimethylheptan-1-ol 
• 100-39-0 benzyl bromide 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 156953-84-3 (3R,9S,11S,13R,14S,16S)-14-hydroxy-3-[(4-hydroxy-3-iodophenyl)methyl]-4,9,11,13-tetramethyl-16-(propan-2-yl)-1-oxa-4,7-diazacyclohexadecane-2,5,8-trione 
• 333354-19-1 (E)-(5S,6R,8R,10S)-11-Benzyloxy-5-hydroxy-2,6,8,10-tetramethyl-undec-2-enoic acid ethyl ester 
• 333354-21-5 (3S,5S,6R,8R,10S)-11-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-2,6,8,10-tetramethyl-undec-1-en-3-ol 
• 333354-20-4 {(2S,3S)-3-[(2S,3R,5R,7S)-8-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-3,5,7-trimethyl-octyl]-2-methyl-oxiranyl}-methanol 
• 333354-25-9 (3R,9S,11S,13R,14S,16S)-14-Hydroxy-3-(3-iodo-4-triisopropylsilanyloxy-benzyl)-16-isopropyl-4,9,11,13-tetramethyl-1-oxa-4,7-diaza-cyclohexadecane-2,5,8-trione 
• 333354-26-0 Trifluoro-acetic acid (3R,9S,11S,13R,14S,16S)-3-(3-iodo-4-triisopropylsilanyloxy-benzyl)-16-isopropyl-4,9,11,13-tetramethyl-2,5,8-trioxo-1-oxa-4,7-diaza-cyclohexadec-14-yl ester 
• 333354-24-8 (2S,4S,6R,7S,9S)-9-[(R)-2-[(2-tert-Butoxycarbonylamino-acetyl)-methyl-amino]-3-(3-iodo-4-triisopropylsilanyloxy-phenyl)-propionyloxy]-7-(tert-butyl-dimethyl-silanyloxy)-2,4,6,10-tetramethyl-undecanoic acid tert-butyl ester 

Relevant academic research and scientific papers

Catalytic, efficient, and syn-selective construction of deoxypolypropionates and other chiral compounds via Zr-catalyzed asymmetric carboalumination of allyl alcohol

An efficient, syn-selective, all catalytic asymmetric protocol for the synthesis of α,ω-diheterofunctional deoxypolypropionates via Zr-catalyzed asymmetric carboalumination (ZACA reaction) was developed. The success of the method critically hinges on the

Total synthesis of antitumor depsipeptide (-)-doliculide.

[reaction: see text] (-)-Doliculide, a potent antitumor agent, is synthesized stereoselectively in a convergent manner. The key strategy involves a stereoselective synthesis of the polyketide unit and synthesis of the D-tyrosine derivative, followed by as