89690-72-2

Upstream product

• 89690-65-3 ethyl 3,4-dihydro-4-hydroxy-1(2H)-pyridinecarboxylate 
• 108-98-5 thiophenol 
• 127619-51-6 ethyl 6-bromo-1,4-dioxa-8-azaspiro<4.5>decane-8-carboxylate 
• 4551-15-9 phenylthiotrimethylsilane 
• 110961-43-8 N-Ethoxycarbonyl-6-methoxy-1,2,3,6-tetrahydropyridine 
• 57330-84-4 ethyl 3,4-dihydro-4-oxo-1(2H)-pyridinecarboxylate 

Relevant academic research and scientific papers

Regioselective Alkylation of Vinylogous N-Acyliminium Ion, Leading to 6-Alkyl-1,2,3,6-tetrahydropyridines, by Using Electrogenerated Acid (EG acid) as a Catalyst

Alkylation of 6-methoxy-1,2,3,6-tetrahydro- and 4-methoxy-1,2,3,4-tetrahydropyridines with organo-silicon compounds as a carbon nucleophile by using electrogenerated acid as an acid catalyst proceeds regioselectively at the C-6 position via vinylogous acy

Synthesis of 2-Substituted Δ3-Piperidines: The Nitrogen Analogue of the Ferrier Rearrangement. An Approach to Streptazolin

The Lewis acid induced reaction of N-carbethoxy-4-hydroxy-1,2,3,4-tetrahydropyridine (6) with various carbon nucleophiles has been studied as a route to 2-substituted Δ3-piperidines