1374407-53-0

Upstream product

• 1374407-42-7 (1R,2R,3R)-3-benzyloxy-2,4-dihydroxy-1-methylbutyl benzoate 
• 1374407-50-7 C₁₂H₁₆O₃ 
• 1374407-40-5 (2R,3S,4R)-4-hydroxy-2-methyltetrahydro-3-furanyl acetate 
• 1374407-56-3 (2R,3R,4R)-4-hydroxy-2-methyl-4-vinyltetrahydro-3-furanyl acetate 
• 143264-39-5 tert-butyl{[(1S)-1-methyl-2-propenyl]oxy}diphenylsilane 
• 1374407-51-8 (2R,3R,4R)-4-(E,3S)-3-{[1-tert-butyl-diphenylsilyl]oxy}-1-butenyl-4-hydroxy-2-methyltetrahydro-3-furanyl acetate 
• 1383609-08-2 C₁₀H₁₈O₅ 
• 1374407-45-0 ethyl 2-{(1S,2R)-1-hydroxy-2-[(4-methoxybenzyl)oxy]propyl}acrylate 
• 1374407-44-9 ethyl 2-[(1S,2R)-2-[(4-methoxybenzyl)oxy]-1-(methoxymethoxy)propyl]acrylate 
• 1374407-54-1 C₂₆H₂₈O₇S 
• 1374407-55-2 (2R,3R,4R)-4-benzyloxy-2-methyltetrahydro-3-furanyl acetate 
• 1374407-46-1 (3S,4R)-3-methoxymethoxy-2-methylenepentane-1,4-diol 
• 1374407-43-8 (2R,3S)-3-methoxymethoxy-2-methyl-4-methylenetetrahydrofuran 
• 1374407-41-6 (2R,3R)-2-methyl-4-oxotetrahydro-3-furanyl acetate 

Relevant academic research and scientific papers

First stereoselective total synthesis of isoaspinonene through a Baylis-Hillman/olefin cross-metathesis protocol

The first stereoselective and efficient total synthesis of isoaspinonene by using Baylis-Hillman reaction, chelation-controlled vinyl Grignard reaction, Wittig olefination, and olefin cross-metathesis reaction of a hitherto unreported substrate as the key