671799-02-3

Upstream product

• 69739-34-0 t-butyldimethylsiyl triflate 
• 671798-77-9 (3R,4S)-1-(4-methoxyphenoxy)-4-methylhex-5-en-3-ol 
• 2653-90-9 1-(but-3-en-1-yloxy)-4-methoxybenzene 
• 479192-15-9 3-(4-methoxyphenoxy)propionaldehyde 

Downstream Products

• 671799-04-5 (4S,5R)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxyphenoxy)-4-methylheptanoic acid pyridin-2-ylmethyl ester 
• 671798-94-0 (2R,3S,5S,6R,8S,9S)-8-[3,5-bis(tert-butyldimethylsilyloxy)phenyl]-2-[2-(4-methoxyphenoxy)ethyl]-3,5,9-trimethyl-1,7-dioxaspiro[5.5]undecane 
• 671798-92-8 (2S,4R,5S)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxyphenoxy)-2,4-dimethylheptanoic acid [(1S,2S)-(2-hydroxy-1-methyl-2-phenylethyl)]methylamide 
• 671798-90-6 (4R,5S)-5-(tert-butyldimethylsilyloxy)-7-(4-methoxyphenoxy)-4-methylheptanoic acid [(1S,2S)-(2-hydroxy-1-methyl-2-phenylethyl)]methylamine 
• 671798-86-0 (3S,5S,6R)-6-[2-(4-methoxyphenoxy)ethyl]-3,5-dimethyltetrahydropyran-2-one 

Relevant academic research and scientific papers

Synthesis of the C16-C35 Fragment of Integramycin Using Olefin Hydroesterification as a Linchpin Reaction

(Matrix presented) The spiroketal unit of the HIV-integrase inhibitor integramycin has been prepared in an efficient and convergent manner. Key steps in this sequence include the use of ruthenium-mediated hydroesterification reactions of homoallylic alcoh