450408-58-9

Upstream product

• 79027-28-4 (2S)-3-(benzyloxy)-2-methylpropanal 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 63930-49-4 (R)-3-(benzyloxy)-2-methylpropan-1-ol 
• 24470-78-8 isopropyltriphenylphosphonium iodide 
• 444109-42-6 (2S,3R,4S)-5-benzyloxy-3-(tert-butyldimethylsilyloxy)-2,4-dimethyl-pentanal 
• 450408-59-0 (4R,2'R,3'S,4'S)-4-benzyl-3-(5'-benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl)-2-oxazolidinone 
• 183506-80-1 (4R,2'R,3'S,4'S)-4-benzyl-3-(5'-benzyloxy-3'-hydroxy-2',4'-dimethylpentanoyl)-2-oxazolidinone 
• 100649-11-4 (2S,3R,4S)-5-Benzyloxy-3-(tert-butyldimethylsilyloxy)-2,4-dimethyl-1-pentanol 
• 74924-27-9 methyl (S)-3-benzyloxy-2-methylpropanoate 

Relevant academic research and scientific papers

Synthetic studies on callipeltin A: Stereoselective synthesis of (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid

An efficient and highly stereocontrolled synthesis of protected (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid, the β-hydroxy acid unit that acylates the N-terminus of callipeltin A, has been devised starting from methyl (2S)-2-methyl-3-hydroxypropion