95682-17-0

Upstream product

• 100-39-0 benzyl bromide 
• 95682-27-2 (1R,2S,3S,4S,5S)-1-Methoxymethoxy-3,5-dimethyl-8-oxo-bicyclo[2.2.2]octane-2-carbaldehyde 
• 95682-13-6 (1S,2R,3S,4R,5R)-1-Methoxymethoxy-3,5-dimethyl-8-oxo-bicyclo[2.2.2]octane-2-carboxylic acid ethyl ester 
• 95682-28-3 (1R,4S,5S,6R,7R)-5-((R)-1-Hydroxy-but-3-enyl)-4-methoxymethoxy-6,7-dimethyl-bicyclo[2.2.2]octan-2-one 
• 95682-15-8 (1R,4S,5S,6R,7R)-5-((R)-1-Benzyloxy-2-oxiranyl-ethyl)-4-methoxymethoxy-6,7-dimethyl-bicyclo[2.2.2]octan-2-one 
• 95682-14-7 (1R,4S,5S,6R,7R)-5-((R)-1-Benzyloxy-but-3-enyl)-4-methoxymethoxy-6,7-dimethyl-bicyclo[2.2.2]octan-2-one 
• 95682-16-9 (1S,2R,4aR,6R,7R,8aR,9R)-2-Benzyloxy-4-hydroxymethyl-8a-methoxymethoxy-7,9-dimethyl-octahydro-1,6-methano-naphthalen-5-one 

Relevant academic research and scientific papers

A NEW SYNTHETIC APPROACH TO THE BICYCLOUNDECANE RING SYSTEM IN TAXANES

The bicycloundecane derivative 19, which was referred to the A,B ring system of taxane diterpenes, was synthesized by a base-induced fragmentation reaction of the tricyclic diol monomesylate 18 derived highly stereoselectively from 5-methyl-1,3-cyc