565193-84-2

Upstream product

• 100-39-0 benzyl bromide 
• 565193-87-5 (2S,3S)-3-(2-methoxy-ethoxymethoxy)-pent-4-en-2-ol 
• 565193-88-6 (2S,3S)-2-benzyloxy-3-(2-methoxyethoxymethoxy)pent-4-ene 
• 565194-39-0 (3S,4S)-4-benzyloxy-3-(2-methoxyethoxymethoxy)pentan-1-ol 

Downstream Products

• 565193-96-6 (2S,3S,5Z,10S)-2-benzyloxy-11-tert-butyldimethylsilyloxy-3-(2-methoxyethoxymethoxy)undec-5-ene 
• 565194-18-5 (2S,3S,5Z,10S,11R)-2-benzyloxy-11,12-bis(tert-butyldimethylsilyloxy)-3-(2-methoxyethoxymethoxy)-10-methyldodec-5-ene 

Relevant academic research and scientific papers

Studies towards the synthesis of epothilone A via organoboranes

Studies towards the synthesis of epothilone A via organoboranes have been described. A modified procedure for the large-scale preparation of B-γ,γ-dimethylallyldiisopinocampheylborane from prenyl alcohol has been developed. This reagent, upon reaction wit

Stereoselective synthesis of the C7-C21 segment of epothilone A via asymmetric alkoxyallyl- and crotylboration

The synthesis of the C7-C21 fragment of epothilone A involving asymmetric alkoxyallyl- and crotylboration using α-pinene-derived reagents is described.