863638-83-9

Upstream product

• 111322-01-1 (R)-1-benzyloxy-hex-5-en-3-ol 
• 7751-38-4 Diisopropylsilyl dichloride 
• 863638-82-8 (1R)-benzyloxy-[1-(2-benzyloxy-ethyl)-but-3-enyloxy]-diisopropyl-silane 
• 863638-78-2 [1-(2-benzyloxy-ethyl)-but-3-enyloxy]-chloro-diisopropyl-silane 

Downstream Products

• 863638-85-1 (4S,6S)-8-benzyloxy-6-(benzyloxy-diisopropyl-silanyloxy)-4-(tert-butyldimethyl-silanyloxy)-octan-2-one 
• 863638-84-0 (4S,6S)-8-benzyloxy-6-(benzyloxy-diisopropyl-silanyloxy)-4-hydroxy-octan-2-one 

Relevant academic research and scientific papers

Towards the combinatorial synthesis of spongistatin fragment libraries by using asymmetric aldol reactions on solid support

By relying on asymmetric boron-mediated aldol reactions, solid phase methodology for the stereoselective synthesis of highly substituted spiroacetals was developed and applied to the preparation of a complex AB-spiroacetal subunit of the antimitotic agent