740853-06-9

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 135362-69-5 3-(4-methoxybenzyl)oxypropan-1-ol 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 
• 96-22-0 pentan-3-one 

Downstream Products

• 740853-07-0 (3R,4S,6R,7R)-3,7-Bis-(tert-butyl-dimethyl-silanyloxy)-1,9-bis-(4-methoxy-benzyloxy)-4,6-dimethyl-nonan-5-one 
• 740852-91-9 (3R,4S,6R,7R)-3-(tert-Butyl-dimethyl-silanyloxy)-7-hydroxy-1,9-bis-(4-methoxy-benzyloxy)-4,6-dimethyl-nonan-5-one 
• 740852-89-5 (4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(4-methoxy-benzyloxy)-4-methyl-heptan-3-one 

Relevant academic research and scientific papers

Asymmetric solid-phase synthesis of 6,6-spiroketals

Structurally simplified spiroketals derived from natural products often retain the biological activity of the parent compound. An asymmetric solid-phase synthesis with boron-mediated aldol reactions as key stereodifferentiating transformations provides 6,