869385-01-3

Upstream product

• 387821-98-9 (R)-4-benzyl-3-((2R,3S,E)-3-hydroxy-2-methyl-5-phenylpent-4-enoyl)oxazolidin-2-one 
• 95585-63-0 (2S,3S)-1,3-dihydroxy-2-methyl-5-phenyl-4-pentene 
• 85908-97-0 5-tert-butoxycarbonylaminopentanoic acid methyl ester 
• 869384-95-2 tert-butyl 3-(tert-butyldimethylsilyloxy)propyl(6-(diethoxyphosphoryl)-5-oxohexyl)carbamate 
• 869385-18-2 5-{tert-butoxycarbonyl-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-amino}-pentanoic acid methyl ester 
• 869384-94-1 (3S,4R,E)-4-(benzyloxy)-3-methyl-6-phenylhex-5-enenitrile 
• 869385-16-0 (2S,3S,E)-3-(benzyloxy)-2-methyl-5-phenylpent-4-en-1-ol 
• 869385-17-1 methyl 5-(allyl(tert-butoxycarbonyl)amino)pentanoate 
• 869385-04-6 (10aS,11R,12S,14aS)-4-tert-butyl 14a-ethyl 11-benzyloxy-12-methyl-9,14-dioxotetradecahydrobenzo[e][1]azacyclododecine-4,14a(1H)-dicarboxylate 

Relevant academic research and scientific papers

Polycyclic molecules from linear precursors: Stereoselective synthesis of clavolonine and related complex structures

(Chemical Equation Presented) A clever way to clavolonine: The total synthesis of the lycopodium alkaloid clavolonine (2) from a linear precursor 1 that contains the complete 16-carbon-atom chain is reported (see scheme). Intramolecular and transannular c