Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes

Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes

碩士 === 國立中正大學 === 化學所 === 94 === To investigate the intramolecular Baylis-Hillman reaction or intermolecular [4+2]cycloaddition reaction by praline-catalyst to get enantioselective products ; based on cycloadditions, we synthesize Ferula-terpenes skeleton via reaction of ? β- unsaturated aldehydes....

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Main Authors: Cheng-Feng Su, 蘇勝豐
Other Authors: B. C. Hong
Format: Others
Language:zh-TW
Published: 2006
Online Access:http://ndltd.ncl.edu.tw/handle/05250778999547082436
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spelling ndltd-TW-094CCU050650382015-10-13T10:45:18Z http://ndltd.ncl.edu.tw/handle/05250778999547082436 Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes 利用proline-催化劑催化?β位置不飽和醛進行環加成反應建構Ferula-terpenes骨架的合成 Cheng-Feng Su 蘇勝豐 碩士 國立中正大學 化學所 94 To investigate the intramolecular Baylis-Hillman reaction or intermolecular [4+2]cycloaddition reaction by praline-catalyst to get enantioselective products ; based on cycloadditions, we synthesize Ferula-terpenes skeleton via reaction of ? β- unsaturated aldehydes. B. C. Hong 洪伯誠 2006 學位論文 ; thesis 295 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立中正大學 === 化學所 === 94 === To investigate the intramolecular Baylis-Hillman reaction or intermolecular [4+2]cycloaddition reaction by praline-catalyst to get enantioselective products ; based on cycloadditions, we synthesize Ferula-terpenes skeleton via reaction of ? β- unsaturated aldehydes.
author2 B. C. Hong
author_facet B. C. Hong
Cheng-Feng Su
蘇勝豐
author Cheng-Feng Su
蘇勝豐
spellingShingle Cheng-Feng Su
蘇勝豐
Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
author_sort Cheng-Feng Su
title Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
title_short Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
title_full Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
title_fullStr Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
title_full_unstemmed Synthetic Approaches toward Ferula-terpenes skeleton via Proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
title_sort synthetic approaches toward ferula-terpenes skeleton via proline-catalyzed cycloadditions of ? β-unsaturated aldehydes
publishDate 2006
url http://ndltd.ncl.edu.tw/handle/05250778999547082436
work_keys_str_mv AT chengfengsu syntheticapproachestowardferulaterpenesskeletonviaprolinecatalyzedcycloadditionsofbunsaturatedaldehydes
AT sūshèngfēng syntheticapproachestowardferulaterpenesskeletonviaprolinecatalyzedcycloadditionsofbunsaturatedaldehydes
AT chengfengsu lìyòngprolinecuīhuàjìcuīhuàbwèizhìbùbǎohéquánjìnxínghuánjiāchéngfǎnyīngjiàngòuferulaterpenesgǔjiàdehéchéng
AT sūshèngfēng lìyòngprolinecuīhuàjìcuīhuàbwèizhìbùbǎohéquánjìnxínghuánjiāchéngfǎnyīngjiàngòuferulaterpenesgǔjiàdehéchéng
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