350046-06-9

Upstream product

• 350046-03-6 3-benzyloxy-2-(3-benzyloxy-propyl)-5-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-tetrahydro-pyran 
• 350046-00-3 (2R,4aR,6S,7R,8aS)-7-Benzyloxy-6-(3-benzyloxy-propyl)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 350045-94-2 (E)-3-{(2R,3R)-3-[(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-phenyl-[1,3]dioxan-4-ylmethyl]-2-methyl-oxiranyl}-acrylic acid methyl ester 
• 350046-01-4 (2R,3S,5R,6S)-5-Benzyloxy-6-(3-benzyloxy-propyl)-2-hydroxymethyl-6-methyl-tetrahydro-pyran-3-ol 
• 350045-97-5 3-((2R,4aR,6S,7R,8aS)-7-Hydroxy-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-propionic acid methyl ester 
• 350045-96-4 (E)-3-((2R,4aR,6S,7R,8aS)-7-Hydroxy-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-acrylic acid methyl ester 
• 350045-95-3 (E)-3-[(2R,3R)-3-((2R,4S,5R)-5-Hydroxy-2-phenyl-[1,3]dioxan-4-ylmethyl)-2-methyl-oxiranyl]-acrylic acid methyl ester 
• 350045-98-6 (2R,4aR,6S,7R,8aS)-6-(3-Hydroxy-propyl)-6-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 100-39-0 benzyl bromide 
• 131310-58-2 (2S,3R)-3-[(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-phenyl-[1,3]dioxan-4-ylmethyl]-2-methyl-oxirane-2-carbaldehyde 
• 350045-93-1 [(2R,3S,5R,6S)-5-Benzyloxy-6-(3-benzyloxy-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-methanol 

Downstream Products

• 350046-08-1 dithiocarbonic acid O-[1-[5-benzyloxy-6-(3-benzyloxy-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-5-(tert-butyl-diphenyl-silanyloxy)-2,4-dimethyl-pent-2-enyl] ester S-methyl ester 
• 350046-07-0 (E)-(R)-1-[(2R,3S,5R,6S)-5-Benzyloxy-6-(3-benzyloxy-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-5-(tert-butyl-diphenyl-silanyloxy)-2,4-dimethyl-pent-2-en-1-ol 

Relevant academic research and scientific papers

Synthesis of the J ring segment of gambieric acid

The J ring segment 2 of gambieric acid was synthesized stereoselectively by the coupling between the cyclic ether component 3 and the alkenyl iodide 4. The tetrahydropyran 3 was stereoselectively synthesized by the 6-endo-cyclization of a hydroxyepoxide prepared from deoxy-D-ribose. The side chain moiety 4 was prepared by the stereoselective hydrostannation of an internal alkyne.