191935-31-6

Upstream product

• 100-39-0 benzyl bromide 
• 219607-75-7 (2R,3R)-2-methyl-1-phenyl-5-hexyn-3-ol 
• 219607-71-3 (2R,3R)-1-(4-methoxybenzyl)oxy-3-methyl-4-phenyl-2-butanol 
• 219607-72-4 (2R,3R)-2-(methanesulfonyl)oxy-1-(4-methoxybenzyl)oxy-3-methyl-4-phenylbutane 
• 219607-70-2 (2S,3S)-2,3-epoxy-1-(4-methoxybenzyl)oxy-4-phenylbutane 
• 219607-73-5 (2R,3R)-2-(methanesulfonyl)oxy-3-methyl-4-phenyl-1-butanol 
• 78571-81-0 (2S-trans)-3-(Phenylmethyl)oxiranemethanol 
• 42238-15-3 (2E)-4-phenylbut-2-en-1-ol 

Downstream Products

• 871514-76-0 (4S,5S)-4-{(R)-[(4R,5S)-5-((5R,6R)-5-Benzyloxy-1-hydroxy-6-methyl-7-phenyl-hept-2-ynyl)-2,2-diethyl-[1,3]dioxolan-4-yl]-ethoxycarbonyl-trimethylsilanyloxy-methyl}-2,2-dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid dimethyl ester 
• 191935-32-7 3-ethyl 1,2-dimethyl (1S,2S,3R,4R,5R,10R,11R)-10-benzyloxy-4,5-(diethylmethylenedioxy)-1,2-(dimethylmethylenedioxy)-11-methyl-6-oxo-12-phenyl-3-(trimethylsilyloxy)-7-dodecyne-1,2,3-tricarboxylate 

Relevant academic research and scientific papers

Facile and efficient preparation of a C-1 side chain equivalent of zaragozic acid C

An optically pure C-1 side chain equivalent of zaragozic acid C, (4R,5R)-4-benzyloxy-5-methyl-6-phenyl-1-hexyne, has been synthesized in ten steps from (E)-4-phenyl-2-buten-1-ol with an overall yield of 50%, involving a Sharpless asymmetric epoxidation as