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AMBIENTUM BIOETHICA BIOLOGIA CHEMIA DIGITALIA DRAMATICA EDUCATIO ARTIS GYMNAST. ENGINEERING EPHEMERIDES EUROPAEA GEOGRAPHIA GEOLOGIA HISTORIA HISTORIA ARTIUM INFORMATICA IURISPRUDENTIA MATHEMATICA MUSICA NEGOTIA OECONOMICA PHILOLOGIA PHILOSOPHIA PHYSICA POLITICA PSYCHOLOGIA-PAEDAGOGIA SOCIOLOGIA THEOLOGIA CATHOLICA THEOLOGIA CATHOLICA LATIN THEOLOGIA GR.-CATH. VARAD THEOLOGIA ORTHODOXA THEOLOGIA REF. TRANSYLVAN
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STUDIA CHEMIA - Ediţia nr.3 din 2020 | |||||||
Articol: |
A STRAIGHTFORWARD SYNTHESIS OF NOVEL 1,3,5-TRIAZINE-BASED MACROCYCLIC SCAFFOLDS. Autori: COSMIN V. CRIŞAN, NICULINA D. HĂDADE, ION GROSU, ANDREEA P. CRIŞAN, ANAMARIA TEREC. |
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Rezumat: DOI: 10.24193/subbchem.2020.3.13 Published Online: 2020-09-30 Published Print: 2020-09-30 pp.171-179 VIEW PDF: FULL PDF ABSTRACT: The synthesis and structural investigation of a series of three macrocycles bearing 2,4,6-tris(p-phenylene)-1,3,5-triazine central units and oligoethyleneoxide bridges are reported. The approach implied the synthesis of non-symmetrical 1,3,5-triazines obtained via a cross-cyclotrimerization reaction, followed by a direct macrocyclization with the corresponding ditosylated oligoethyleneglycols. The obtained non-symmetrically C-substituted 1,3,5-triazines macrocycles were characterized by NMR spectroscopy and High-Resolution Mass Spectrometry (HRMS). Key words: macrocycles, 1,3,5-triazine, cross-cyclotrimerization, oligoethylene bridges |
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