935746-68-2

Upstream product

• 3937-56-2 1,9-Nonanediol 
• 2746-25-0 p-Methoxybenzyl bromide 
• 531513-01-6 9-(4-methoxy-benzyloxy)-nonanal 
• 267005-80-1 9-(4-methoxybenzyloxy)nonan-1-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 
• 935746-64-8 (E)-ethyl 11-(4-methoxybenzyloxy)undec-2-enoate 
• 935746-67-1 ((4S,5S)-5-(8-(4-methoxybenzyloxy)octyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol 

Downstream Products

• 935746-69-3 (S)-11-(4-methoxybenzyloxy)undec-1-yn-3-ol 
• 935746-70-6 ((S)-11-(4-methoxybenzyloxy)undec-1-yn-3-yloxy)(tert-butyl)diphenylsilane 
• 935746-73-9 (9S,12S,13S,E)-9-(tert-butyldiphenylsilyloxy)-octadec-10-ene-1,12,13-triol 
• 935746-74-0 (S,E)-9-(tert-butyldiphenylsilyloxy)-11-((4S,5S)-2,2-dimethyl-5-pentyl-1,3-dioxolan-4-yl)undec-10-en-1-ol 
• 935746-75-1 (S,E)-9-(tert-butyldiphenylsilyloxy)-11-((4S,5S)-2,2-dimethyl-5-pentyl-1,3-dioxolan-4-yl)undec-10-enoic acid 
• 935746-71-7 ((S,E)-1-(4-methoxybenzyloxy)octadec-12-en-10-yn-9-yloxy)(tert-butyl)diphenylsilane 
• 935746-72-8 (6S,7S,10S)-10-(tert-butyldiphenylsilyloxy)-18-(4-methoxybenzyloxy)octadec-8-yne-6,7-diol 
• 947304-85-0 C₃₄H₅₄SiO₄C₃H₂ 
• 947304-75-8 (S,E)-1-(4-methoxybenzyloxy)octadec-12-en-10-yn-9-ol 
• 947304-76-9 (S,10E,12E)-1-(4-methoxybenzyloxy)octadeca-10,12-dien-9-ol 
• 947304-77-0 ((S,10E,12E)-1-(4-methoxybenzyloxy)-octadeca-10,12-dien-9-yloxy)(tert-butyl)diphenylsilane 
• 947304-78-1 (S,10E,12E)-9-(tert-butyldiphenylsilyloxy)-octadeca-10,12-dien-1-ol 
• 947304-86-1 C₁₈H₃₂O₂SiC₁₆H₁₈ 
• 947304-79-2 C₁₈H₃₂O₃SiC₁₆H₁₈ 

Relevant academic research and scientific papers

Enantioselective synthesis of (-)-pinellic acid

An enantioselective convergent approach toward the total synthesis of pinellic acid 1 from 1,9-nonanediol is described. The synthetic strategy features iterative Sharpless asymmetric dihydroxylation, Sonogashira coupling and Birch reduction.

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.