164365-93-9

Upstream product

• 164365-92-8 N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-<3-<(tert-butyldimethylsilyl)oxy>propyl>amine 
• 164365-87-1 <11(2S)>-11-<2-piperidyl>>-9-undecenoic acid 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 164365-91-7 N-<(benzyloxy)carbonyl>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-<3-<(tert-butyldimethylsilyl)oxy>propyl>amine 
• 164365-86-0 methyl <11(2S)>-11-<2-piperidinyl>>-9-undecenoate 
• 164365-90-6 N-<(benzyloxy)carbonyl>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(3-hydroxypropyl)amine 
• 164365-89-3 N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(3-hydroxypropyl)amine 
• 164365-88-2 tert-butyl 4-bromobutylcarbamate 
• 143264-48-6 <2R,2(1S),3aS>-2-<1-<(tert-butyldiphenylsilyl)oxy>-2-methylpropyl>-3,3a,4,5,6,7-hexahydro-2H-isoxazolo<2,3-a>pyridine 
• 143264-54-4 (2S)-N-<(benzyloxy)carbonyl>-2-(formylmethyl)piperidine 
• 173425-07-5 <2S,2(2R),2(3S)>-N-<(benzyloxy)carbonyl>-2-(2,3-dihydroxy-4-methylpentyl)piperidine 
• 173425-05-3 <2R,2(1S),3aS>-2-(1-hydroxy-2-methylpropyl)-3,3a,4,5,6,7-hexahydro-2H-isoxazolo<2,3-a>pyridine 
• 173425-06-4 <2S,2(2R),2(3S)>-2-(2,3-dihydroxy-4-methylpentyl)piperidine 
• 34418-91-2 2,3,4,5-tetrahydropyridine N-oxide 

Downstream Products

• 164365-95-1 <11(2S)>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(2-formylethyl)-11-<2-piperidyl>>-9-undecenamide 
• 21008-79-7 Oncinotin 
• 164365-94-0 <11(2S)>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(3-hydroxypropyl)-11-<2-piperidyl>-9-undecenamide 

Relevant academic research and scientific papers

Enantioselective total synthesis of the macrocyclic spermidine alkaloid (-)-oncinotine

The macrocyclic spermidine alkaloid (-)-oncinotine (1), isolated from Oncinotis nitida (Apocynaceae), was synthesized enantioselectively for the first time based on intramolecular iminium ion cyclization utilizing enantiomerically pure (2S)-N-[(benzyloxy)

The chiral total synthesis of (-)-oncinotine

The first chiral synthesis of (-)-oncinotine 1 in natural form has been achieved starting from the protected (S)-N-benzyloxycarbonyl-2-piperidylacetaldehyde 3 based on a new route involving 17-membered ring formation via iminium cyclization, which establi