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...

Full description

Bibliographic Details
Main Authors: TUNG CHAO, 趙瞳
Other Authors: Ming-Jung Wu
Format: Others
Language:zh-TW
Published: 2018
Online Access:http://ndltd.ncl.edu.tw/handle/vjczqa
id ndltd-TW-106NSYS5065013
record_format oai_dc
spelling 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
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 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.
author2 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 AT tungchao facilesynthesisofdibenzosuberonesviapalladiumiicatalyzedintramolecularchactivationcccouplingoforthoaroylated35diarylisoxazole
AT zhàotóng facilesynthesisofdibenzosuberonesviapalladiumiicatalyzedintramolecularchactivationcccouplingoforthoaroylated35diarylisoxazole
AT tungchao yǐèrjiàbǎjīnshǔcuīhuàlínwèiběnxījī35èrběnjīyìězuòzhīfēnzinèitànqīngjiànhuóhuàtàntànjiànǒuhéhéchéngduìèrběnbìngsāifēntóngzhīyǎnshēngwùyánjiū
AT zhàotóng yǐèrjiàbǎjīnshǔcuīhuàlínwèiběnxījī35èrběnjīyìězuòzhīfēnzinèitànqīngjiànhuóhuàtàntànjiànǒuhéhéchéngduìèrběnbìngsāifēntóngzhīyǎnshēngwùyánjiū
_version_ 1719284448172703744