900796-48-7

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 220430-05-7 2-(1-hydroxy-3-p-methoxybenzyloxypropyl)acrylic acid methyl ester 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 

Downstream Products

• 900796-49-8 2-[1-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-propyl]-propenal 
• 900796-51-2 4-[1-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-propyl]-penta-2,4-dienal 
• 900796-50-1 4-[1-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-propyl]-penta-2,4-dienoic acid methyl ester 
• 900796-62-5 (E)-(2S,3R,7S)-1-((S)-4-Benzyl-5,5-diphenyl-2-thioxo-oxazolidin-3-yl)-7-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-9-(4-methoxy-benzyloxy)-2-methyl-6-methylene-non-4-en-1-one 
• 900796-61-4 (E)-(2S,3R,7R)-1-((S)-4-Benzyl-5,5-diphenyl-2-thioxo-oxazolidin-3-yl)-7-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-9-(4-methoxy-benzyloxy)-2-methyl-6-methylene-non-4-en-1-one 

Relevant academic research and scientific papers

A Baylis-Hillman approach to the synthesis of C1-C11 fragment of caribenolide I

Stereoselective synthesis of C1-C11 fragment of caribenolide I, a potent antitumour macrolide isolated from a marine dinoflagellate Amphidinium sp. is described. The key steps rely on asymmetric aldol reactions, to control the absolu