Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes

碩士 === 高雄醫學大學 === 醫藥暨應用化學研究所碩士班 === 94 === In this thesis, a novel route for the synthesis of substituted cyanonaphthalenes was described. The synthetic strategy was started from isovanillin and through a sequence of reactions including O-allylation、Claisen rearrangement、O-alkylation、Baylis-Hillman...

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Main Authors:	Po-Yuan Chen, 陳伯淵
Other Authors:	王英基
Format:	Others
Language:	zh-TW
Published:	2006
Online Access:	http://ndltd.ncl.edu.tw/handle/37366667358827056017

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spelling	ndltd-TW-094KMC055370212015-12-16T04:32:13Z http://ndltd.ncl.edu.tw/handle/37366667358827056017 Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes 從異位香草素經由Claisen轉位、Baylis-Hillman反應與閉環歧化反應新路徑合成多取代的腈萘類化合物 Po-Yuan Chen 陳伯淵碩士高雄醫學大學醫藥暨應用化學研究所碩士班 94 In this thesis, a novel route for the synthesis of substituted cyanonaphthalenes was described. The synthetic strategy was started from isovanillin and through a sequence of reactions including O-allylation、Claisen rearrangement、O-alkylation、Baylis-Hillman reaction, and ring-closing metathesis to produce title compounds 5-alkoxy-6-methoxynaphthalene-2-carbonitrile, in high yields. 王英基 2006 學位論文 ; thesis 53 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碩士班 === 94 === In this thesis, a novel route for the synthesis of substituted cyanonaphthalenes was described. The synthetic strategy was started from isovanillin and through a sequence of reactions including O-allylation、Claisen rearrangement、O-alkylation、Baylis-Hillman reaction, and ring-closing metathesis to produce title compounds 5-alkoxy-6-methoxynaphthalene-2-carbonitrile, in high yields.
author2	王英基
author_facet	王英基 Po-Yuan Chen 陳伯淵
author	Po-Yuan Chen 陳伯淵
spellingShingle	Po-Yuan Chen 陳伯淵 Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
author_sort	Po-Yuan Chen
title	Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
title_short	Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
title_full	Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
title_fullStr	Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
title_full_unstemmed	Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
title_sort	sequential claisen rearrangement/baylis-hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes
publishDate	2006
url	http://ndltd.ncl.edu.tw/handle/37366667358827056017
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Sequential Claisen rearrangement/Baylis-Hillman reaction/ring closing metathesis from isovanillin as a new route for the synthesis of substituted cyanonaphthalenes

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