1374763-99-1

Upstream product

• 1374763-96-8 (2S,4R,5R,6R)-5-(benzyloxy)-N-[(1S,2S)-1-hydroxy-1-phenylpropan-2-yl]-N,2,4-trimethyl-6-[(4R,5R)-2,2,5-trimethyl-1,3-dioxan-4-yl]heptanamide 
• 1374763-97-9 (2S,4R,5R,6R)-5-(benzyloxy)-2,4-dimethyl-6-[(4R,5R)-2,2,5-trimethyl-1,3-dioxan-4-yl]heptan-1-ol 
• 75-29-6 isopropyl chloride 
• 1374763-98-0 C₂₃H₃₇IO₃ 
• 1374763-95-7 (4R,5R)-4-[(2R,3S,4S)-3-(benzyloxy)-5-iodo-4-methylpentan-2-yl]-2,2,5-trimethyl-1,3-dioxane 
• 77-76-9 2,2-dimethoxy-propane 

Relevant academic research and scientific papers

Enantioselective total synthesis of (+)- and (-)-vittatalactone

The asymmetric total synthesis of both enantiomers of (+)- and (-)-vittatalactone has been achieved using a desymmetrization strategy to create three methyl chiral centers. The key steps in these total syntheses are Myers asymmetric alkylation, copper-cat