869385-10-4

Upstream product

• 387821-98-9 (R)-4-benzyl-3-((2R,3S,E)-3-hydroxy-2-methyl-5-phenylpent-4-enoyl)oxazolidin-2-one 
• 179690-97-2 5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester 
• 95585-63-0 (2S,3S)-1,3-dihydroxy-2-methyl-5-phenyl-4-pentene 
• 14273-92-8 methyl 5-hydroxypentanoate 
• 542-28-9 3,4,5,6-tetrahydro-2H-pyran-2-one 
• 869385-08-0 (5S,6R,E)-tert-butyl 6-benzyloxy-13-(tert-butyldiphenylsilyloxy)-5-methyl-3,9-dioxotridec-7-enoate 
• 869385-05-7 (3S,4R,E)-4-benzyloxy-11-(tert-butyldiphenylsilyloxy)-3-methyl-7-oxoundec-5-enenitrile 
• 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 
• 869385-09-1 (2S,3R,4S)-tert-butyl 3-benzyloxy-2-(6-(tert-butyldiphenylsilyloxy)-2-oxohexyl)-4-methyl-6-oxocyclohexanecarboxylate 
• 107-13-1 acrylonitrile 

Downstream Products

• 869385-14-8 (4aR,5S,6R,7S)-tert-butyl 6-benzyloxy-5-(6-(tert-butyldiphenylsilyloxy)-2-oxohexyl)-7-methyl-2,3,4,4a,5,6,7,8-octahydroquinoline-4a-carboxylate 

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