117452-71-8

Upstream product

• 100-39-0 benzyl bromide 
• 22520-29-2 (2α(S*),3α)-(+/-)-α,3-Dimethyloxiranemethanol 
• 57984-70-0 Pent-3-yn-2-ol 

Downstream Products

• 117452-72-9 (2R,3S,4S)-4-Benzyloxy-1-(diphenyl-phosphinoyl)-2-methyl-pentan-3-ol 
• 140654-13-3 (2S,3S,4R)-2-Benzyloxy-4-iodo-pentan-3-ol 
• 117452-72-9 (2R,3S,4S)-4-Benzyloxy-1-(diphenyl-phosphinoyl)-2-methyl-pentan-3-ol 
• 117475-68-0 ((2S,3S,4S,6S)-6-{(2S,3S,4S,6S)-6-[(1S,2R)-1-((S)-1-Benzyloxy-ethyl)-3-(diphenyl-phosphinoyl)-2-methyl-propoxy]-4-methoxy-2-methyl-tetrahydro-pyran-3-yloxy}-4-methoxy-2-methyl-tetrahydro-pyran-3-yloxy)-tert-butyl-dimethyl-silane 
• 117452-75-2 (2S,3S,4S,6S)-6-[(1S,2R)-1-((S)-1-Benzyloxy-ethyl)-3-(diphenyl-phosphinoyl)-2-methyl-propoxy]-4-methoxy-2-methyl-tetrahydro-pyran-3-ol 

Relevant academic research and scientific papers

APPROACHES TO AVERMECTIN ASSEMBLY: ELABORATION OF AN α-L-OLEANDROSYL-α-L-OLEANDROSIDE DERIVATIVE

A stereospecific synthesis of the disaccharide moiety of avermectin A2b has been accomplished in 11 steps from commercially available 3-pentyn-2-ol and L-rhamnal.