197379-09-2

Upstream product

• 40458-77-3 8-oxabicyclo[3.2.1]oct-6-en-3-one 
• 100-39-0 benzyl bromide 
• 99327-44-3 exo-8-oxabicyclo[3.2.1]oct-6-en-3-ol 

Downstream Products

• 1357384-44-1 (2S,4S,6R)-4-(benzyloxy)-2-((Z)-2-butoxyvinyl)-6-vinyltetrahydro-2H-pyran 
• 1357384-45-2 (2S,4S,6R)-4-(benzyloxy)-2-((Z)-2-(4-methoxyphenoxy)vinyl)-6-vinyltetrahydro-2H-pyran 
• 1357384-77-0 2-((2S,4S,6S)-4-(benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)ethanol 
• 1357384-76-9 2-((2S,4S,6S)-4-(benzyloxy)-6-((Z)-2-butoxyvinyl)tetrahydro-2H-pyran-2-yl)ethanol 
• 1133432-03-7 (2S,4S,6R)-4-(benzyloxy)-2-(Z)-styryl-6-vinyltetrahydro-2H-pyran 
• 786695-72-5 (2S,4S,6R)-4-(benzyloxy)-2-(E)-styryl-6-vinyltetrahydro-2H-pyran 
• 198475-85-3 (1S,5S,7R)-7-benzyloxy-2,9-dioxabicyclo[3.3.1]nonan-3-one 
• 198475-81-9 (1S,3R,5R)-3-benzyloxy-8-oxabicyclo[3.2.1]octan-6-one 
• 198475-79-5 (1S,3R,5R,6S)-3-benzyloxy-8-oxabicyclo[3.2.1]octan-6-ol 

Relevant academic research and scientific papers

8-Oxabicyclo[3.2.1]oct-6-en-3-one as a module for the synthesis of β-alkoxy-δ-valerolactones relevant to natural products and drugs

The enantioselective synthesis of all four stereoisomeric cia-3,5 and trans-3.5-substituted β-alkoxy-δ-valerolactones was accomplished starting from 8-oxabicyclo[3.2.1]oct-6-en-3-one.