637002-71-2

Upstream product

• 128461-65-4 3-(p-methoxybenzyloxy)propanal 

Downstream Products

• 637002-77-8 (3E,8E)-(2S,7R)-7-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-11-methyl-dodeca-3,8-dien-5-one 
• 637002-78-9 (E)-(2S,7R)-7-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-11-methyl-dodec-8-en-5-one 
• 943897-94-7 C₄₆H₆₄O₅Si₂ 
• 943898-26-8 C₃₀H₄₆O₅Si 
• 943898-25-7 C₂₇H₄₄O₁₀S 
• 943898-27-9 C₂₆H₄₂O₈ 
• 943898-24-6 C₄₂H₆₀O₈Si 
• 943897-92-5 C₃₈H₅₂O₆Si 
• 943897-91-4 C₃₈H₅₀O₆Si 
• 943897-90-3 C₁₅H₂₀O₄ 

Relevant academic research and scientific papers

Enantioselective Total Synthesis of (+)-Leucascandrolide A Macrolactone

(Matrix presented) The enantioselective synthesis of the (+)-leucascandrolide A macrolactone has been achieved in 20 linear steps from 1,3-propanediol. The key steps in the synthesis are a reductive cleavage of bicyclic ketal 5 to establish the C15 stereo