Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole
碩士 === 國立中山大學 === 化學系研究所 === 106 === Compounds containing the dibenzosuberone skeleton always show diverse biological activities, hence we are interesting in developing synthetic methodology for affording novel dibenzosuberone derivatives by using the compound, phenyl(2-(5-phenylisoxazol-3-yl)phenyl...
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ndltd-TW-106NSYS50650132019-10-31T05:22:27Z http://ndltd.ncl.edu.tw/handle/vjczqa Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole 以二價鈀金屬催化鄰位-苯醯基-3,5-二苯基異噁唑之分子內碳-氫鍵活化/碳-碳鍵偶合合成對二苯并噻吩酮之衍生物研究 TUNG CHAO 趙瞳 碩士 國立中山大學 化學系研究所 106 Compounds containing the dibenzosuberone skeleton always show diverse biological activities, hence we are interesting in developing synthetic methodology for affording novel dibenzosuberone derivatives by using the compound, phenyl(2-(5-phenylisoxazol-3-yl)phenyl)methanone, that had been synthesised earlier in our lab. A method via palladium-catalyzed C-H activation for the synthesis of dibenzosuberones derivatives from phenyl(2-(5-phenylisoxazol-3-yl)phenyl)methanone was presented in this report. Furthermore, the dibenzosuberone products also bearing a isoxazole group, so we can expect that it will apply for drug development and also show good tolerance of functional groups. Ming-Jung Wu 吳明忠 2018 學位論文 ; thesis 355 zh-TW |
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碩士 === 國立中山大學 === 化學系研究所 === 106 === Compounds containing the dibenzosuberone skeleton always show diverse biological activities, hence we are interesting in developing synthetic methodology for affording novel dibenzosuberone derivatives by using the compound, phenyl(2-(5-phenylisoxazol-3-yl)phenyl)methanone, that had been synthesised earlier in our lab. A method via palladium-catalyzed C-H activation for the synthesis of dibenzosuberones derivatives from phenyl(2-(5-phenylisoxazol-3-yl)phenyl)methanone was presented in this report. Furthermore, the dibenzosuberone products also bearing a isoxazole group, so we can expect that it will apply for drug development and also show good tolerance of functional groups.
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Ming-Jung Wu |
author_facet |
Ming-Jung Wu TUNG CHAO 趙瞳 |
author |
TUNG CHAO 趙瞳 |
spellingShingle |
TUNG CHAO 趙瞳 Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
author_sort |
TUNG CHAO |
title |
Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
title_short |
Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
title_full |
Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
title_fullStr |
Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
title_full_unstemmed |
Facile Synthesis of Dibenzosuberones via Palladium(II)-Catalyzed Intramolecular C-H Activation/C-C Coupling of Ortho-Aroylated 3,5-Diarylisoxazole |
title_sort |
facile synthesis of dibenzosuberones via palladium(ii)-catalyzed intramolecular c-h activation/c-c coupling of ortho-aroylated 3,5-diarylisoxazole |
publishDate |
2018 |
url |
http://ndltd.ncl.edu.tw/handle/vjczqa |
work_keys_str_mv |
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