Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon
The thermolysis of the 1:1-cycloadduct 3, synthesized by the addition of cyclopentadienequinone (1) and 3-methyl-2,4-diphenyl-5-oxazolone (2), yields 5,6-dihydro-2-methyl-1,3-diphenyl-2H-isoindol-4,7-dione (5) and not the tetracyclic diketone 4 (cf. [2]). The structure of 5 is elucidated by spectra...
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| Format: | Article |
| Language: | deu |
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Swiss Chemical Society
1977-04-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9347 |
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| _version_ | 1850170710678306816 |
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| author | Josef Lukáč Heinz Heimgartner Hans Schmid |
| author_facet | Josef Lukáč Heinz Heimgartner Hans Schmid |
| author_sort | Josef Lukáč |
| collection | DOAJ |
| description |
The thermolysis of the 1:1-cycloadduct 3, synthesized by the addition of cyclopentadienequinone (1) and 3-methyl-2,4-diphenyl-5-oxazolone (2), yields 5,6-dihydro-2-methyl-1,3-diphenyl-2H-isoindol-4,7-dione (5) and not the tetracyclic diketone 4 (cf. [2]). The structure of 5 is elucidated by spectral data and by dehydrogenation to the 2 H-isoindole-4,7-dione 6.
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| format | Article |
| id | doaj-art-2c54b167e5524d8fa78e3df00f3910a7 |
| institution | OA Journals |
| issn | 0009-4293 2673-2424 |
| language | deu |
| publishDate | 1977-04-01 |
| publisher | Swiss Chemical Society |
| record_format | Article |
| series | CHIMIA |
| spelling | doaj-art-2c54b167e5524d8fa78e3df00f3910a72025-08-20T02:20:26ZdeuSwiss Chemical SocietyCHIMIA0009-42932673-24241977-04-0131410.2533/chimia.1977.138Thermolyse des 1:1-Adduktes aus «Münchnon» und CyclopentadienchinonJosef Lukáč0Heinz Heimgartner1Hans Schmid2Organisch-chemisches Institut der Universität ZürichOrganisch-chemisches Institut der Universität ZürichOrganisch-chemisches Institut der Universität Zürich The thermolysis of the 1:1-cycloadduct 3, synthesized by the addition of cyclopentadienequinone (1) and 3-methyl-2,4-diphenyl-5-oxazolone (2), yields 5,6-dihydro-2-methyl-1,3-diphenyl-2H-isoindol-4,7-dione (5) and not the tetracyclic diketone 4 (cf. [2]). The structure of 5 is elucidated by spectral data and by dehydrogenation to the 2 H-isoindole-4,7-dione 6. https://www.chimia.ch/chimia/article/view/9347 |
| spellingShingle | Josef Lukáč Heinz Heimgartner Hans Schmid Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon CHIMIA |
| title | Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon |
| title_full | Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon |
| title_fullStr | Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon |
| title_full_unstemmed | Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon |
| title_short | Thermolyse des 1:1-Adduktes aus «Münchnon» und Cyclopentadienchinon |
| title_sort | thermolyse des 1 1 adduktes aus munchnon und cyclopentadienchinon |
| url | https://www.chimia.ch/chimia/article/view/9347 |
| work_keys_str_mv | AT joseflukac thermolysedes11adduktesausmunchnonundcyclopentadienchinon AT heinzheimgartner thermolysedes11adduktesausmunchnonundcyclopentadienchinon AT hansschmid thermolysedes11adduktesausmunchnonundcyclopentadienchinon |