632339-41-4

Upstream product

• 632339-29-8 (3R,4S,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-4-hydroxy-3-methyl-tetrahydro-pyran-2-one 
• 632339-28-7 (2R,3S,5S)-7-(tert-Butyl-diphenyl-silanyloxy)-3,5-dihydroxy-2-methyl-heptanoic acid 
• 632339-26-5 (2R,3S,5S)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3,5,7-trihydroxy-2-methyl-heptan-1-one 
• 632339-30-1 4-(tert-butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran-2-one 
• 632339-25-4 (2R,3S)-4-((S)-2,2-Dimethyl-[1,3]dioxan-4-yl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-hydroxy-2-methyl-butan-1-one 
• 632339-34-5 {4-(tert-butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran-2-yl}-methanol 
• 632339-32-3 2-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran 
• 632339-38-9 (Z)-3-{(2R,3S,4S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran-2-yl}-2-methyl-acrylic acid ethyl ester 
• 632339-31-2 2-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran-2-ol 
• 632339-27-6 (2R,3S,5S)-7-(tert-Butyl-diphenyl-silanyloxy)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3,5-dihydroxy-2-methyl-heptan-1-one 
• 632339-24-3 (R)-4-(2-Benzyloxy-ethyl)-2,2-dimethyl-[1,3]dioxane 
• 225786-18-5 (S)-2-(2,2-dimethyl-1,3-dioxan-4-yl)ethanal 
• 185553-79-1 (R)-2-<2,2-dimethyl-1,3-dioxan-4-yl>ethan-1-ol 
• 81132-13-0 (S)-5-phenylmethoxypentane-1,3-diol 

Downstream Products

• 632339-42-5 (2E,4Z)-5-{(2R,3S,4S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-tetrahydro-pyran-2-yl}-4-methyl-penta-2,4-dienoic acid ethyl ester 

Relevant academic research and scientific papers

Enantioselective construction of the C1-C16 segment of lasonolide A

An efficient and enantiocontrolled synthesis of the C1-C 16 segment of lasonolide A has been accomplished starting from a readily available optically pure aldehyde.