100571-45-7

Upstream product

• 100571-19-5 6-((tert-butyldimethylsilyl)oxy)hex-2-ynal 
• 100571-28-6 methyl (E)-4-methyl-6-(benzyloxy)-1-vinyl-4-hexenyl dithiocarbonate 
• 69857-25-6 methyl (E)-3-methyl-6-(tetrahydropyranyloxy)-2-hexenoate 
• 5390-04-5 pent-1-yn-5-ol 
• 61362-77-4 5-[tert-butyldimethylsilyloxy]pent-1-yne 
• 32989-52-9 (E)-4-methyl-6-(phenylmethoxy)-4-hexenal 
• 51755-88-5 methyl (E)-6-hydroxy-3-methyl-2-hexenoate 
• 100571-29-7 (E,E)-6-methyl-8-(benzyloxy)-2,6-octadien-1-ol 
• 69857-26-7 (E)-3-methyl-6-(tetrahydropyranyloxy)-2-hexen-1-ol 
• 100571-26-4 (E)-3-methyl-6-(tetrahydropyranyloxy)-2-hexenyl benzyl ether 
• 100571-27-5 methyl (E,E)-6-methyl-8-(benzyloxy)-2,6-octadienoate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 100571-18-4 6-(tert-butyldimethylsiloxy)hex-2-yn-1-ol 
• 98066-00-3 (E)-4-methyl-6-(phenylmethoxy)-4-hexen-1-ol 

Relevant academic research and scientific papers

The Synthesis of Cembranolide Precursors via Addition of Allylstannanes to Conjugated Aldehydes

The Lewis acid promoted addition of functionalized allylstannanes A9, C10, and C11 to a variety of conjugated aldehydes was examined as a possible route to acyclic precursors of macrocyclic diterpenoids.Additions to crotonaldehyde proceeded as expected, g