1448445-89-3

Upstream product

• 1448445-86-0 C₁₁H₂₀O₃ 
• 1448445-87-1 C₂₇H₃₈O₃Si 
• 303044-40-8 (2E,5R)-5-{[(1,1-dimethylethyl)diphenylsilyl]oxy}hex-2-en-1-ol 
• 303044-41-9 (2R,3R)-3-{(2R)-2-{[(1,1-dimethylethyl)diphenylsilyl]oxy}propyl}oxirane-2-methanol 
• 303044-46-4 (-)-(2R,3R,5R)-5-(tert-butyldiphenylsilyloxy)-2,3-(oxiranyl)-hexan-1-al 
• 303044-42-0 (2R,3R)-2-{(2R)-2-{[(1,1-dimethylethyl)diphenylsilyl]oxy}propyl}-3-ethenyloxirane 
• 1448445-88-2 (3S,4R,6R)-6-{[(1,1-dimethylethyl)diphenylsilyl]oxy}hept-1-ene-3,4-diol 
• 77-76-9 2,2-dimethoxy-propane 
• 133906-65-7 (2E,5R)-hex-2-ene-1,5-diol 
• 1161160-10-6 ethyl (5R)-5-hydroxyhex-2-ynoate 

Downstream Products

• 356043-22-6 multiplolide A 

Relevant academic research and scientific papers

Stereoselective total synthesis of multiplolide A and of a diastereoisomer

A stereoselective total synthesis of multiplolide A (1) and of its diastereoisomer 2 was described from easily accessible starting materials (Schemes 2-4). The synthetic strategy involves a Jacobsen resolution, Sharpless epoxidation, Swern oxidation, Yamaguchi reaction, and ring-closing metathesis (RCM). Copyright