63598-39-0

Upstream product

• 119238-15-2 1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexitol 
• 51450-45-4 (2R,3S)-2-hydroxymethyltetrahydropyran-3-ol 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 119116-55-1 O-(1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexityl) S-methyl dithiocarbonate 
• 100-52-7 benzaldehyde 

Downstream Products

• 119116-61-9 O-benzyl-enantio-ineupatoriol 
• 175777-60-3 (R)-2-[2-((2R,3S)-3-Benzyloxy-tetrahydro-pyran-2-yl)-ethyl]-dihydro-pyran-3-one 
• 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 
• 175664-11-6 (2R,3S,2R,3S)-2-<2'-<3-(benzyloxy)tetrahydropyran-2-yl>ethyl>tetrahydropyran-3-ol 
• 175664-08-1 3(S)-(benzyloxy)tetrahydropyran-2-one 
• 119116-57-3 (2R,3S)-3-(benzyloxy)tetrahydropyran-2-carbaldehyde 
• 119116-56-2 (2R,3S)-<3-(benzyloxy)tetrahydropyran-2-yl>methanol 

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

A CONVERGENT SYNTHESIS OF THE O-BENZYL DERIVATIVE OF ENANTIO-INEUPATORIOL FROM A CARBOHYDRATE PRECURSOR

The trans-2,3-disubstituted tetrahydropyran 7, obtained in eight steps from methyl α-D-glucoside, and the phosphonium salt 10, obtained from thiophene in six steps, were successfully combined in a Wittig reaction to form 11, the O-benzyl enantiomer of the