727411-53-2

Upstream product

• 727411-52-1 (4R)-6-(4-methoxybenzyloxy)-4-methylhex-2-yne 
• 768-33-2 phenyldimethylsilyl chloride 
• 727411-51-0 (R)-4-((4-methoxybenzyl)oxy)-2-methylbutan-1-ol 
• 172668-98-3 (3R)-4-(tert-butyldimethylsilanyloxy)-3-methylbutyronitrile 
• 158817-24-4 (3R)-1,1-dibromo-4-(4-methoxybenzyloxy)-3-methylpent-1-ene 
• 320740-01-0 (R)-4-(4-methoxybenzyloxy)-2-methylbutanal 
• 156757-31-2 (3R)-4-(tert-butyldimethylsilanyloxy)-3-methylbutyraldehyde 
• 147915-55-7 (3R)-4-(tert-butyldimethylsilanyloxy)-3-methylbutan-1-ol 
• 727411-50-9 (2R)-1-(tert-butyl(dimethyl)silyloxy)-4-(4-methoxybenzyloxy)-2-methylbutane 

Downstream Products

• 727411-55-4 (3R,4E)-3-methyl-5-(dimethyl(phenyl)silyl)hex-4-en-1-yl 2',2'-dimethylpropionate 
• 727411-54-3 (3R,4E)-5-(dimethyl(phenyl)silyl)-3-methylhex-2-en-1-ol 

Relevant academic research and scientific papers

Stereoselective synthesis of the hydrophobic side chain of scyphostatin

The hydrophobic side chain of scyphostatin was synthesized by a convergent synthetic pathway. The key reactions were the enzymatic asymmetric acetylation of a meso-diol, construction of the C12′-C13′ trisubstituted E-olefin moiety by Negishi coupling, and