Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine

Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine

碩士 === 國立中興大學 === 化學系所 === 105 === This thesis describes the investigation of aromatic-mediated domino Rh- catalyzed hydroformylation bicyclization, which has been developed for rapid preparation of medicinally-interesting alkaloids. The first part is focused on the scope and limitation study using...

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Main Authors: Tai-Hung Yang, 楊泰泓
Other Authors: 邱文華
Format: Others
Language:zh-TW
Published: 2017
Online Access:http://ndltd.ncl.edu.tw/handle/93120025157741154640
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spelling ndltd-TW-105NCHU50650562017-11-12T04:39:01Z http://ndltd.ncl.edu.tw/handle/93120025157741154640 Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine 關於以芳香環控制之骨牌式銠催化雙環化反應與葉底珠屬植物鹼Securinine之合成研究 Tai-Hung Yang 楊泰泓 碩士 國立中興大學 化學系所 105 This thesis describes the investigation of aromatic-mediated domino Rh- catalyzed hydroformylation bicyclization, which has been developed for rapid preparation of medicinally-interesting alkaloids. The first part is focused on the scope and limitation study using various substrste, comprising of allylamide, homoallylamide, and 3-butenamide derivatives bearing 3,4-dimethoxybenzene or 3,4,5-trimethoxybenzene moiety. The second part we used furan-mediated domino hydroformylation bicyclization to synthesize Securinine skeleton. 邱文華 2017 學位論文 ; thesis 173 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立中興大學 === 化學系所 === 105 === This thesis describes the investigation of aromatic-mediated domino Rh- catalyzed hydroformylation bicyclization, which has been developed for rapid preparation of medicinally-interesting alkaloids. The first part is focused on the scope and limitation study using various substrste, comprising of allylamide, homoallylamide, and 3-butenamide derivatives bearing 3,4-dimethoxybenzene or 3,4,5-trimethoxybenzene moiety. The second part we used furan-mediated domino hydroformylation bicyclization to synthesize Securinine skeleton.
author2 邱文華
author_facet 邱文華
Tai-Hung Yang
楊泰泓
author Tai-Hung Yang
楊泰泓
spellingShingle Tai-Hung Yang
楊泰泓
Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
author_sort Tai-Hung Yang
title Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
title_short Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
title_full Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
title_fullStr Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
title_full_unstemmed Investigation on Aromatic-mediated Domino Rh-Catalyzed Hydroformylation Double Cyclization and Synthetic Studies on Securinega Alkaloid Securinine
title_sort investigation on aromatic-mediated domino rh-catalyzed hydroformylation double cyclization and synthetic studies on securinega alkaloid securinine
publishDate 2017
url http://ndltd.ncl.edu.tw/handle/93120025157741154640
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AT yángtàihóng investigationonaromaticmediateddominorhcatalyzedhydroformylationdoublecyclizationandsyntheticstudiesonsecurinegaalkaloidsecurinine
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