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  • The reaction of 3-phenylaminocyclopent-2-en-1-one with 4-methyl, 4-methoxy and 4-chlorobenzenediazonium tetrafluoroborates was used to prepare the azo coupling products 3a-c. It was found out that these compounds are present in both CDCl3 solution and solid phase practically exclusively as (E)-3-phenylamino-2-(4-subst.phenyldiazenyl)cyclopent-2-en-1-ones with N?H???N intramolecular hydrogen bond. The substitution of the phenyl residue of the diazonium salt has no effect on the position of the tautomeric equilibrium. On the other hand, the compounds 4a,b formed by the reaction of 3-phenylamino-1H-inden-1-one with 4-methylbenzene- or benzenediazonium tetrafluoroborates exist in CDCl3 solution and in solid phase as hydrazone compounds. In the solution they occur as a mixture of three forms, out of which two were identified as E/Z isomers with different types of hydrogen bonds. Compound 5 formed by the reaction of 3-amino-5,5-dimethylcyclohex-2-en-1-one with 4-methoxybenzenediazonium tetrafluoroborate is
  • The reaction of 3-phenylaminocyclopent-2-en-1-one with 4-methyl, 4-methoxy and 4-chlorobenzenediazonium tetrafluoroborates was used to prepare the azo coupling products 3a-c. It was found out that these compounds are present in both CDCl3 solution and solid phase practically exclusively as (E)-3-phenylamino-2-(4-subst.phenyldiazenyl)cyclopent-2-en-1-ones with N?H???N intramolecular hydrogen bond. The substitution of the phenyl residue of the diazonium salt has no effect on the position of the tautomeric equilibrium. On the other hand, the compounds 4a,b formed by the reaction of 3-phenylamino-1H-inden-1-one with 4-methylbenzene- or benzenediazonium tetrafluoroborates exist in CDCl3 solution and in solid phase as hydrazone compounds. In the solution they occur as a mixture of three forms, out of which two were identified as E/Z isomers with different types of hydrogen bonds. Compound 5 formed by the reaction of 3-amino-5,5-dimethylcyclohex-2-en-1-one with 4-methoxybenzenediazonium tetrafluoroborate is (en)
  • Reakcí 3-fenylaminocyklopent-2-en-1-onu s 4-methyl, 4-methoxy a 4-chlorbenzendiazonium-tetrafluorboráty byly připraveny azokopulační produkty 3a-c. Bylo zjištěno, že tyto sloučeniny existují jak v roztoku CDCl3, tak i v pevné fázi prakticky jako (E)-3-fenylamino-2-(4-subst.fenyldiazenyl)cyklopent-2-en-1-ony s N?H???N intramolekulární vodíkovou vazbou. Substituce na diazoniové soli nemá vliv na polohu tautomerní rovnováhy. Sloučeniny 4a,b vzniklé reakcí 3-fenylamino-1H-inden-1-onu s 4-methylbenzen nebo benzendiazonium-tetrafluorborátem jsou v roztoku CDCl3 i v pevné fázi jako hydrazosloučeniny. V roztoku tvoří tři formy, z nichž dvě byly identifikovány jako E/Z izomery lišící se typem vodíkových vazeb. Sloučenina 5 vzniklá reakcí 3-amino-5,5-dimethylcyklohex-2-en-1-onu s 4-methoxybenzendiazonium-tetrafluorborátu byla převedena na stabilní hydrochlorid 5?HCl stáním v chloroformu; tento produkt vykazuje vysoký stupeň delokalizace kladného náboje. Její struktura byla studována X-ray. (cs)
Title
  • Synthesis and Structure of Some Azo Coupled Cyclic beta-Enaminones
  • Synthesis and Structure of Some Azo Coupled Cyclic beta-Enaminones (en)
  • Příprava a struktura některých azokopulovaných cyklických beta-enaminonů (cs)
skos:prefLabel
  • Synthesis and Structure of Some Azo Coupled Cyclic beta-Enaminones
  • Synthesis and Structure of Some Azo Coupled Cyclic beta-Enaminones (en)
  • Příprava a struktura některých azokopulovaných cyklických beta-enaminonů (cs)
skos:notation
  • RIV/00216275:25310/07:00006564!RIV08-MSM-25310___
http://linked.open.../vavai/riv/strany
  • 330-339
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021627501)
http://linked.open...iv/cisloPeriodika
  • 4
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 453899
http://linked.open...ai/riv/idVysledku
  • RIV/00216275:25310/07:00006564
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • 1H; 13C; 15N NMR; azo coupling; tautomerism; enaminones; X-Ray; NMR (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [D5E09C0F1FF3]
http://linked.open...i/riv/nazevZdroje
  • Magnetic Resonance in Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 45
http://linked.open...iv/tvurceVysledku
  • Šimůnek, Petr
  • Lyčka, Antonín
  • Macháček, Vladimír
  • Svobodová, Markéta
  • Bertolasi, Valerio
  • Lusková, Lucie
http://linked.open...n/vavai/riv/zamer
issn
  • 0749-1581
number of pages
http://localhost/t...ganizacniJednotka
  • 25310
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