Rearrangement in the systems ethyl bromopyruvate-1-(cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine as an effi cient approach to 4,5,6,7-tetrahydroindoles
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DOI: 10.1007/s11172-019-2512-5
Abstract: Abstract1-(Cyclohex-1-enyl)piperidine, -pyrrolidine, and -morpholine react with ethyl bromopyruvate in refluxing dioxane to afford the corresponding 4,5,6,7-tetrahydroindole derivatives. Possibility to convert the synthesized compounds into their aromatic counterparts was exemplified by one model compound. read more here.
Keywords: pyrrolidine morpholine; cyclohex enyl; enyl piperidine; ethyl bromopyruvate ... See more keywords
Potential of Small Molecules Piperidine and Pyrrolidine Against Copper-Resistant Xanthomonas perforans, Causal Agent of Bacterial Spot of Tomato.
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DOI: 10.1094/pdis-04-24-0929-re
Abstract: Bacterial spot of tomato (BST), caused by Xanthomonas perforans, is an economically important disease of tomatoes in Florida. Due to the heavy reliance on copper-based bactericides for control of BST, copper-resistant strains of X. perforans… read more here.
Keywords: bacterial spot; piperidine pyrrolidine; disease; control ... See more keywords
Synthesis of piperidine and pyrrolidine derivatives by electroreductive cyclization of imine with terminal dihaloalkanes in a flow microreactor
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DOI: 10.3762/bjoc.18.39
Abstract: We have successfully synthesized piperidine and pyrrolidine derivatives by electroreductive cyclization using readily available imine and terminal dihaloalkanes in a flow microreactor. Reduction of the substrate imine on the cathode proceeded efficiently due to the… read more here.
Keywords: electroreductive cyclization; pyrrolidine derivatives; derivatives electroreductive; piperidine pyrrolidine ... See more keywords