947304-79-2

Upstream product

• 531513-01-6 9-(4-methoxy-benzyloxy)-nonanal 
• 267005-80-1 9-(4-methoxybenzyloxy)nonan-1-ol 
• 66-25-1 hexanal 
• 60595-37-1 (E)-1-iodohept-1-ene 
• 3937-56-2 1,9-Nonanediol 
• 947304-78-1 (S,10E,12E)-9-(tert-butyldiphenylsilyloxy)-octadeca-10,12-dien-1-ol 
• 947304-77-0 ((S,10E,12E)-1-(4-methoxybenzyloxy)-octadeca-10,12-dien-9-yloxy)(tert-butyl)diphenylsilane 
• 947304-76-9 (S,10E,12E)-1-(4-methoxybenzyloxy)octadeca-10,12-dien-9-ol 
• 947304-75-8 (S,E)-1-(4-methoxybenzyloxy)octadec-12-en-10-yn-9-ol 
• 935746-65-9 (2R,3S)-ethyl 11-(4-methoxybenzyloxy)-2,3-dihydroxyundecanoate 
• 935746-66-0 (4R,5S)-ethyl 5-(8-(4-methoxybenzyloxy)octyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 935746-68-2 (4S,5R)-4-(8-(4-methoxybenzyloxy)octyl)-5-(chloromethyl)-2,2-dimethyl-1,3-dioxolane 
• 935746-67-1 ((4S,5S)-5-(8-(4-methoxybenzyloxy)octyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol 
• 935746-64-8 (E)-ethyl 11-(4-methoxybenzyloxy)undec-2-enoate 

Relevant academic research and scientific papers

Enantioselective syntheses of (-)-pinellic acid, α- and β-dimorphecolic acid

An efficient enantioselective convergent approach for the synthesis of (-)-pinellic acid 1, α- and β-dimorphecolic acid (2 and 3) from 1,9-nonane diol is described. The synthetic strategy features Sharpless asymmetric hydroxylation, Sonogashira coupling and Birch reduction.