175777-60-3

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 119116-56-2 (2R,3S)-<3-(benzyloxy)tetrahydropyran-2-yl>methanol 
• 119116-57-3 (2R,3S)-3-(benzyloxy)tetrahydropyran-2-carbaldehyde 
• 440083-07-8 (S)-3-Benzyloxy-2-[(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-ylethynyl]-tetrahydro-pyran-2-ol 
• 175664-10-5 (2R,3S,2'R,3'S)-<2-<3'-(benzyloxy)tetrahydropyran-2'-yl>ethynyl>tetrahydropyran-3-ol 
• 175664-06-9 (2R,3S)-2-(2',2'-dibromovinyl)-3-(tert-butyldimethylsiloxy)-tetrahydropyran 
• 175664-08-1 3(S)-(benzyloxy)tetrahydropyran-2-one 
• 125877-83-0 (2'S,3'S)-3'-(tert-butyldimethylsiloxy)-tetrahydropyran-2'-carbaldehyde 
• 138750-71-7 (2'R,3'S)-<3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-yl>methanol 
• 63598-39-0 (2R,4aR,8aS)-2-phenylhexahydropyrano<3,2-d>-1,3-dioxin 
• 175664-11-6 (2R,3S,2R,3S)-2-<2'-<3-(benzyloxy)tetrahydropyran-2-yl>ethyl>tetrahydropyran-3-ol 

Relevant academic research and scientific papers

Simple designs for the construction of complex trans-fused polyether toxin frameworks. A convergent strategy based on hydroxy ketone cyclization of C-linked oxacycles

A single, unified convergent strategy for the stereocontrolled synthesis of trans-fused polyethers was developed. It was demonstrated that the epimerization and reductive intramolecular coupling of hydroxy ketones in reactions with silane - Lewis acids (S