302969-13-7

Upstream product

• 82299-37-4 benzyloxy-2 piperonal 
• 100-39-0 benzyl bromide 
• 302969-11-5 2-[1-(4-Benzyloxy-benzo[1,3]dioxol-5-yl)-meth-(E)-ylidene]-piperidine-1-carboxylic acid tert-butyl ester 
• 302968-94-1 2-(benzo-1,3-dioxol-5-yl)-1,3-dimethylimidazolidine 
• 223477-90-5 1-tert-butoxycarboxy-2-diphenylphosphinylpiperidine 
• 175857-65-5 2-(diphenylphosphinoyl)piperidine 
• 23780-59-8 4-hydroxybenzo[d][1,3]dioxole-5-carbaldehyde 
• 120-57-0 piperonal 
• 522-33-8 Tripiperidin 
• 14588-61-5 4-benzyloxy-3,5-dimethoxybenzoic acid chloride 
• 302969-12-6 2-(4-benzyloxy-benzo[1,3]dioxol-5-ylmethyl)-piperidine 

Relevant academic research and scientific papers

First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin

The benzoindolizidine and-quinolizidine analogues of α- and β-peltatin were designed and synthesized by two different synthetic routes involving as the key step the Bischler-Napieralski cyclization of suitably substituted N-acyl-2-arylmethylpyrrolidine and -piperidine derivatives. The in vitro biological activity of these analogues as well as some of their derivatives was subsequently evaluated. Copyright (C) 2000 Elsevier Science Ltd.