257280-74-3

Upstream product

• 257280-70-9 Acetic acid 2-[(2R,4aR,6S,7R,8aS)-7-(tert-butyl-dimethyl-silanyloxy)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl]-ethyl ester 
• 257280-71-0 Acetic acid 2-((2R,4aR,6S,7R,8aS)-7-hydroxy-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-ethyl ester 
• 131310-64-0 [(2R,4aR,6S,7R,8aS)-7-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl]-acetaldehyde 
• 131310-63-9 2-[(2R,4aR,6S,7R,8aS)-7-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl]-ethanol 
• 257280-72-1 (E)-3-[(2R,4aR,6S,7R,8aS)-6-(2-Acetoxy-ethyl)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy]-acrylic acid ethyl ester 

Downstream Products

• 257280-75-4 (E)-3-[(2R,4aR,6S,7R,8aS)-6-Methyl-6-(2-oxo-ethyl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy]-acrylic acid ethyl ester 

Relevant academic research and scientific papers

Stereoselective syntheses of trans-fused 6,6- and 6,7-membered ether ring systems having an angular methyl group based on SmI2-induced reductive intramolecular cyclization

Highly stereoselective syntheses of trans-fused 6,6- and 6,7-membered ether ring systems having an angular methyl group were achieved based on SmI2-induced reductive intramolecular cyclizations of an aldehyde or a methyl ketone and a β-alkoxy a