164365-91-7

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 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 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 164365-94-0 <11(2S)>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(3-hydroxypropyl)-11-<2-piperidyl>-9-undecenamide 
• 164365-95-1 <11(2S)>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-(2-formylethyl)-11-<2-piperidyl>>-9-undecenamide 
• 164365-93-9 <11(2S)>-N-<4-<(tert-butoxycarbonyl)amino>butyl>-N-<3-<(tert-butyldimethylsilyl)oxy>propyl>-11-<2-piperidyl>-9-undecenamide 
• 21008-79-7 Oncinotin 

Relevant academic research and scientific papers

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

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)