Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals

碩士 === 國立中興大學 === 化學系所 === 107 === Aryl imidazolium ionic liquids successfully catalyzed Friedel−Crafts acylation, thioesterification, per-O-acetylation, and regioselective reductive ring opening of benzylidene acetals in the sealed tubes. These reactions can form a C−C bond, a C−S bond, a C−O bond,...

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Main Authors:	Yao-Peng Wu, 巫耀朋
Other Authors:	Shun-Yuan Luo
Format:	Others
Language:	zh-TW
Published:	2019
Online Access:	http://ndltd.ncl.edu.tw/handle/7sw7sz

id	ndltd-TW-107NCHU5065035
record_format	oai_dc
spelling	ndltd-TW-107NCHU50650352019-11-29T05:36:25Z http://ndltd.ncl.edu.tw/handle/7sw7sz Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals 芳基咪唑離子液體催化Friedel-Crafts醯化、硫酯化、乙醯化和亞芐基縮醛的區域選擇性還原開環 Yao-Peng Wu 巫耀朋碩士國立中興大學化學系所 107 Aryl imidazolium ionic liquids successfully catalyzed Friedel−Crafts acylation, thioesterification, per-O-acetylation, and regioselective reductive ring opening of benzylidene acetals in the sealed tubes. These reactions can form a C−C bond, a C−S bond, a C−O bond, and C−H bond with high atom economy. Two ionic liquids exhibited high activity and catalyzed essential reactions with good to excellent yields. Shun-Yuan Luo 羅順原 2019 學位論文 ; thesis 142 zh-TW
collection	NDLTD
language	zh-TW
format	Others
sources	NDLTD
description	碩士 === 國立中興大學 === 化學系所 === 107 === Aryl imidazolium ionic liquids successfully catalyzed Friedel−Crafts acylation, thioesterification, per-O-acetylation, and regioselective reductive ring opening of benzylidene acetals in the sealed tubes. These reactions can form a C−C bond, a C−S bond, a C−O bond, and C−H bond with high atom economy. Two ionic liquids exhibited high activity and catalyzed essential reactions with good to excellent yields.
author2	Shun-Yuan Luo
author_facet	Shun-Yuan Luo Yao-Peng Wu 巫耀朋
author	Yao-Peng Wu 巫耀朋
spellingShingle	Yao-Peng Wu 巫耀朋 Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
author_sort	Yao-Peng Wu
title	Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
title_short	Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
title_full	Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
title_fullStr	Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
title_full_unstemmed	Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
title_sort	aryl imidazolium ionic liquid−catalyzed friedel−crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals
publishDate	2019
url	http://ndltd.ncl.edu.tw/handle/7sw7sz
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Aryl imidazolium ionic liquid−catalyzed Friedel−Crafts acylation, thioesterification, acetylation, and regioselective reductive ring opening of benzylidene acetals

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