740845-40-3

Upstream product

• 740845-35-6 2-{[(2R,3R)-3-(tert-butyldimethylsilyloxy)-tetrahydro-2H-pyran-2-yl]methoxy}acetic acid 
• 740845-32-3 [(2R,3R)-3-(tert-butyldimethylsilyloxy)-tetrahydro-2H-pyran-2-yl]methanol 
• 51450-46-5 (2R,3R)-2-(hydroxymethyl)tetrahydro-2H-pyran-3-ol 
• 918958-20-0 3-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran 
• 864719-92-6 [(2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-ylmethoxy]-acetic acid benzyl ester 

Downstream Products

• 740845-43-6 (2R,3R)-2-{[(benzyloxycarbonyl)methoxy]methyl}-tetrahydro-2H-pyran-3-yl 2-{[(2R,3R)-3-(tert-butyldimethylsilyloxy)-tetrahydro-2H-pyran-2-yl]methoxy}acetate 
• 864719-73-3 benzyl 2-{[(2R,3R)-3-(2-{[(2R,3R)-3-hydroxy-tetrahydro-2H-pyran-2-yl]methoxy}acetoxy)-tetrahydro-2H-pyran-2-yl]methoxy}acetate 

Relevant academic research and scientific papers

Synthesis and antiproliferative activity of (2R,3R)-disubstituted tetrahydropyrans. Part 2: Effect of side chain homologation

In this study, we synthesized a series of enantiomerically pure (2R,3R)- and (2R,3S)-disubstituted tetrahydropyrans bearing a CH2O spacer group on the side chain at position 2 of the heterocyclic ring. The in vitro antiproliferative activities

Synthesis and cation complexation properties of new macrolides

The cis-2-alkyl-3-oxy-tetrahydropyran unit as a novel structure for the design and synthesis of a new type of ionophores with C2-symmetry is reported. The synthesis of seven different macrolides and a crown ether and their cation complexation p

The cis-2-alkyl-3-oxy-tetrahydropyran unit as a building block for new ionophores with C2-symmetry

The use of cis-2-alkyl-3-oxy-tetrahydropyran unit is reported as a novel structure for the design and synthesis of a new type of ionophore with C 2-symmetry. The synthesis of five macrolides and their complexation properties were investigated.