1,n-Diamines. Part 4: synthesis of 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1,3-diazocines

In this Letter we present the synthesis of hitherto unreported 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1,3-diazocines 1. Cyclic amidines 1 were synthesized by PPSE promoted ring closure of N-acyl-N′-arylpentamethylenediamines 2. The cyclodehydration reaction was performed under microwave irradiation in...

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Veröffentlicht in:Tetrahedron letters 2011-11, Vol.52 (48), p.6443-6445
Hauptverfasser: Díaz, Jimena E., Gruber, Nadia, Orelli, Liliana R.
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creator Díaz, Jimena E.
Gruber, Nadia
Orelli, Liliana R.
description In this Letter we present the synthesis of hitherto unreported 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1,3-diazocines 1. Cyclic amidines 1 were synthesized by PPSE promoted ring closure of N-acyl-N′-arylpentamethylenediamines 2. The cyclodehydration reaction was performed under microwave irradiation in solvent-free conditions. Precursors 2 were prepared by selective functionalization of N-arylcadaverines 3.
doi_str_mv 10.1016/j.tetlet.2011.09.097
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subjects Chemistry
Closures
Cyclic amidines
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
Irradiation
Medium size heterocycles
Microwaves
Organic chemistry
Polyamine analogs
PPSE
Precursors
Preparations and properties
Synthesis (chemistry)
Tetrahedrons
title 1,n-Diamines. Part 4: synthesis of 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1,3-diazocines
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