202405-18-3

Upstream product

• 100-39-0 benzyl bromide 
• 202405-28-5 (R)-9-(tert-Butyl-dimethyl-silanyloxy)-nonan-2-ol 
• 202405-17-2 Butyric acid (R)-8-(tert-butyl-dimethyl-silanyloxy)-1-methyl-octyl ester 
• 202405-16-1 9-(tert-Butyl-dimethyl-silanyloxy)-nonan-2-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 91898-32-7 8-(tert-butyldimethylsiloxy)octan-1-ol 
• 128622-13-9 8-(tert-butyl)dimethylsilyloxyoctanal 
• 629-41-4 1,8-Octanediol 

Downstream Products

• 202405-25-2 (E)-(R)-8-Acetoxy-15-benzyloxy-hexadec-2-en-6-ynoic acid ethyl ester 
• 202405-22-9 (6RS,13R)-6-acetoxy-13-benzyloxy-1-tetrahydropyranyloxytetradec-4-yne 
• 202405-21-8 (6RS,13R)-6-hydroxy-13-benzyloxy-1-tetrahydropyranyloxytetradec-4-yne 
• 202405-24-1 (6RS,13R)-6-acetoxy-13-benzyloxytetradec-4-ynal 
• 202405-23-0 (6RS,13R)-6-acetoxy-13-benzyloxytetradec-4-yn-1-ol 
• 202405-20-7 (8R)-8-benzyloxynonanal 
• 202405-19-4 (8R)-8-benzyloxynonan-1-ol 

Relevant academic research and scientific papers

Enantiomeric synthesis of the key synthon of the oviposition-deterring pheromone of Rhagoletis cerasi L.

A convenient and enantioselective synthesis of ethyl (8RS,15R)-6-acetoxy-15-hydroxyhexadecanoate 15 via a chemoenzymatic approach has been described.The salient features of the synthesis were operational simplicity, use of easily accessible materials, and