164672-08-6

Upstream product

• 160798-31-2 (2R,4aR,5S)-5-Benzyloxy-2-ethyl-2,4a,5,6,7,8-hexahydropyrido<1,2-b><1,2>oxazin-8-one 
• 160728-56-3 (4E,6E,3S)-3-Benzyloxynona-4,6-dienyl toluene-p-sulfonate 
• 160728-61-0 (2R,4aR,5S)-5-Benzyloxy-2-ethyl-2,3,4,4a,5,6,7,8-octahydropyrido<1,2-b><1,2>oxazin-8-one 
• 160728-60-9 (5E,7E,4S)-4-Benzyloxy-N-hydroxyocta-5,7-dienamide 
• 160728-57-4 (5E,7E,4S)-4-Benzyloxydeca-5,7-dienenitrile 
• 160728-59-6 Methyl (5E,7E,4S)-4-benzyloxydeca-5,7-dienoate 
• 160728-58-5 (5E,7E,3S)-4-Benzyloxydeca-5,7-dienoic acid 
• 160728-55-2 (4E,6E,3S)-3-Benzyloxynona-4,6-dienol 
• 145958-02-7 (2S,4S)-2-phenyl-1,3-dioxane-4-carboxaldehyde 
• 7348-72-3 trans-Pent-2-enyl(triphenyl)phosphonium bromide 
• 160728-62-1 (2R,4aR,5S,8S)-5-Benzyloxy-2-ethyl-8-propyl-2,3,4,4a,5,6,7,8-octahydropyrido<1,2-b><1,2>oxazin 

Downstream Products

• 58117-91-2 (-)-pumiliotoxin C hydrochloride 
• 160798-33-4 (2S,4aS,5R,8aR)-1-Benzyl-5-methyl-2-propyldecahydroquinoline 
• 160728-67-6 (2S,8aR)-1-Benzoyl-5-methyl-2-propyl-1,2,3,4,6,7,8,8a-octahydroquinolin-6-one 
• 160728-68-7 (2S,4aS,5R,8aR)-1-Benzoyl-5-methyl-2-propyldecahydroquinolin-6-one 
• 160728-64-3 (2R,3S,6S)-1-Benzoyl-2-<(3R)-3-hydroxypentyl>-6-propylpiperidine-3-ol 
• 160728-65-4 (2R,6S)-1-Benzoyl-2-(3-oxopentyl)-6-propylpiperidine-3-one 
• 178740-06-2 (2S,4aS,5S,8aR)-1-Benzyl-5-methyl-2-propyldecahydroquinoline 
• 160728-63-2 (2R,3S,6S)-1-Benzoyl-3-benzyloxy-2-<(3R)-3-hydroxypentyl>-6-propylpiperidine 

Relevant academic research and scientific papers

Stereoselective total synthesis of (-)-pumiliotoxin C by an aqueous intramolecular acylnitroso Diels-Alder approach

A chiral approach to (-)-pumiliotoxin C based on an aqueous intramolecular acylnitroso Diels-Alder reaction is described. Upon treatment of the (S)-1,3-diene hydroxamic acid 19, available from L-malic acid, with Pr4NIO4 under the aqu

Total synthesis of (-)-pumiliotoxin C by aqueous intramolecular acylnitroso Diels-Alder approach

A chiral approach to (-)-pumiliotoxin C via a stereoselective intramolecular hetero Diels-Alder reaction of a chiral acylnitroso compound performed in an aqueous medium is described.