339563-80-3

Upstream product

• 339563-56-3 7-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-decanoic acid ethyl ester 
• 339563-78-9 7-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-decanal 
• 339563-68-7 4,8-bis-(tert-butyl-dimethyl-silanyloxy)-oct-1-ene 
• 339563-77-8 7-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-decanoic acid ethyl ester 
• 339563-70-1 5-(tert-butyl-dimethyl-silanyloxy)-octan-1-ol 
• 339563-50-7 5-(tert-butyl-dimethyl-silanyloxy)-oct-7-en-1-ol 
• 339563-66-5 8-(tert-butyl-dimethyl-silanyloxy)-oct-1-en-4-ol 
• 339563-51-8 5-(tert-butyl-dimethyl-silanyloxy)-octanal 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 87184-80-3 5-tert-butyldimethylsilyloxypentanal 

Relevant academic research and scientific papers

Synthesis of a 2,9-dioxabicyclo[3.3.1]nonane via double intramolecular hetero-Michael addition: entry to the F-G ring system of the azaspiracids.

[structure: see text]. An effective approach to form a 1,3-disubstituted 2,9-dioxabicyclo[3.3.1]nonane system representing the core of the F and G rings (C28-C34) of the azaspiracid natural products has been developed. The double intramolecular hetero-Mic