A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate
碩士 === 高雄醫學大學 === 醫藥暨應用化學研究所 === 102 === A facile and efficient approach to synthesis β-ketoamides from β-enaminoesters via Ag(I) catalysis is described. A first catalytic protocol has been developed with broad substrate scope in good to excellent yields. The cross over experimentssuggested that the...
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Others |
Language: | zh-TW |
Published: |
2014
|
Online Access: | http://ndltd.ncl.edu.tw/handle/2dh4d6 |
id |
ndltd-TW-102KMC05537025 |
---|---|
record_format |
oai_dc |
spelling |
ndltd-TW-102KMC055370252019-05-15T21:43:13Z http://ndltd.ncl.edu.tw/handle/2dh4d6 A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate 藉由三氟甲基磺酸銀催化合成β-酮醯胺 Cheng-Tien Hsiao 蕭呈恬 碩士 高雄醫學大學 醫藥暨應用化學研究所 102 A facile and efficient approach to synthesis β-ketoamides from β-enaminoesters via Ag(I) catalysis is described. A first catalytic protocol has been developed with broad substrate scope in good to excellent yields. The cross over experimentssuggested that the reaction underwent a new pathway and not through the traditional condensation intermediates ethyl benzoylacetateand aniline. In this reaction the C-O and C-N bond formations were undergone to give the desired compound. A gram scale synthesis was successfully demonstrated with the optimized reaction conditions. Jeh-Jeng Wang 王志鉦 2014 學位論文 ; thesis 135 zh-TW |
collection |
NDLTD |
language |
zh-TW |
format |
Others
|
sources |
NDLTD |
description |
碩士 === 高雄醫學大學 === 醫藥暨應用化學研究所 === 102 === A facile and efficient approach to synthesis β-ketoamides from β-enaminoesters via Ag(I) catalysis is described. A first catalytic protocol has been developed with broad substrate scope in good to excellent yields. The cross over experimentssuggested that the reaction underwent a new pathway and not through the traditional condensation intermediates ethyl benzoylacetateand aniline. In this reaction the C-O and C-N bond formations were undergone to give the desired compound. A gram scale synthesis was successfully demonstrated with the optimized reaction conditions.
|
author2 |
Jeh-Jeng Wang |
author_facet |
Jeh-Jeng Wang Cheng-Tien Hsiao 蕭呈恬 |
author |
Cheng-Tien Hsiao 蕭呈恬 |
spellingShingle |
Cheng-Tien Hsiao 蕭呈恬 A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
author_sort |
Cheng-Tien Hsiao |
title |
A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
title_short |
A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
title_full |
A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
title_fullStr |
A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
title_full_unstemmed |
A Facile Entry to Synthesis β-Ketoamides from β-Enaminoesters Catalysed by Silver (I) Triflate |
title_sort |
facile entry to synthesis β-ketoamides from β-enaminoesters catalysed by silver (i) triflate |
publishDate |
2014 |
url |
http://ndltd.ncl.edu.tw/handle/2dh4d6 |
work_keys_str_mv |
AT chengtienhsiao afacileentrytosynthesisbketoamidesfrombenaminoesterscatalysedbysilveritriflate AT xiāochéngtián afacileentrytosynthesisbketoamidesfrombenaminoesterscatalysedbysilveritriflate AT chengtienhsiao jíyóusānfújiǎjīhuángsuānyíncuīhuàhéchéngbtóngxīàn AT xiāochéngtián jíyóusānfújiǎjīhuángsuānyíncuīhuàhéchéngbtóngxīàn AT chengtienhsiao facileentrytosynthesisbketoamidesfrombenaminoesterscatalysedbysilveritriflate AT xiāochéngtián facileentrytosynthesisbketoamidesfrombenaminoesterscatalysedbysilveritriflate |
_version_ |
1719118988505513984 |