About: Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones     Goto   Sponge   NotDistinct   Permalink

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Description
  • Substituted 3-hydroxyquinoline-2,4(1H,3H)-diones 3 were transformed into 3-acyloxy-1,3-dihydro-2H indol-2-ones 4 and isomeric 4-acyl-1,4-dihydro-3,1-benzoaxazin-2-ones 5.The influence of the substituents and the reaction conditions on the course of the reaction was studied. In the proposed mechanism a double rearrangement takes place.
  • Substituted 3-hydroxyquinoline-2,4(1H,3H)-diones 3 were transformed into 3-acyloxy-1,3-dihydro-2H indol-2-ones 4 and isomeric 4-acyl-1,4-dihydro-3,1-benzoaxazin-2-ones 5.The influence of the substituents and the reaction conditions on the course of the reaction was studied. In the proposed mechanism a double rearrangement takes place. (en)
Title
  • Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones
  • Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones (en)
skos:prefLabel
  • Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones
  • Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones (en)
skos:notation
  • RIV/00216305:26520/00:63400007!RIV/2001/MSM/265201/N
http://linked.open.../vavai/riv/strany
  • A-1551
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM 265200015)
http://linked.open...iv/cisloPeriodika
  • March
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
  • Klásek, Antonín
  • Polis, Jiří
  • Kořistek, Kamil
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 728695
http://linked.open...ai/riv/idVysledku
  • RIV/00216305:26520/00:63400007
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • rearrangements, mechanisms, benzoxazines, indolinones, quinolinones (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [D93BA409E00B]
http://linked.open...i/riv/nazevZdroje
  • Tetrahedron
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 56
http://linked.open...iv/tvurceVysledku
  • Košmrlj, Janez
  • Klásek, Antonín
  • Polis, Jiří
  • Kořistek, Kamil
http://linked.open...n/vavai/riv/zamer
issn
  • 0040-4020
number of pages
http://localhost/t...ganizacniJednotka
  • 26520
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