Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application

Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application

碩士 === 國立中正大學 === 化學暨生物化學研究所 === 104 === We use (E)-2-(2-nitrovinyl)phenol and aldehyde for the synthesis of hexahydro-6H-benzo[c]chromenones via enantioselective organocatalytic domino Michael-acetalization-Henry reaction, and construct four chiral centers in one step with excellent enantiosele...

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Main Authors: Hsieh, Yu-You, 謝雨祐
Other Authors: Hong, Bor-Cherng
Format: Others
Language:zh-TW
Published: 2015
Online Access:http://ndltd.ncl.edu.tw/handle/pfz88t
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spelling ndltd-TW-104CCU000650042019-05-15T22:25:32Z http://ndltd.ncl.edu.tw/handle/pfz88t Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application Hsieh, Yu-You 謝雨祐 碩士 國立中正大學 化學暨生物化學研究所 104 We use (E)-2-(2-nitrovinyl)phenol and aldehyde for the synthesis of hexahydro-6H-benzo[c]chromenones via enantioselective organocatalytic domino Michael-acetalization-Henry reaction, and construct four chiral centers in one step with excellent enantioselectivity. Then the enantio-enrich hexahydro-6H-benzo[c]chromenones was transformed to the Aflatoxins analogs via a sequence of reduction and Nef reaction. Hong, Bor-Cherng 洪伯誠 2015 學位論文 ; thesis 443 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立中正大學 === 化學暨生物化學研究所 === 104 === We use (E)-2-(2-nitrovinyl)phenol and aldehyde for the synthesis of hexahydro-6H-benzo[c]chromenones via enantioselective organocatalytic domino Michael-acetalization-Henry reaction, and construct four chiral centers in one step with excellent enantioselectivity. Then the enantio-enrich hexahydro-6H-benzo[c]chromenones was transformed to the Aflatoxins analogs via a sequence of reduction and Nef reaction.
author2 Hong, Bor-Cherng
author_facet Hong, Bor-Cherng
Hsieh, Yu-You
謝雨祐
author Hsieh, Yu-You
謝雨祐
spellingShingle Hsieh, Yu-You
謝雨祐
Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
author_sort Hsieh, Yu-You
title Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
title_short Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
title_full Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
title_fullStr Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
title_full_unstemmed Enantioselective organocatalytic domino Michael-acetalization-Henry reaction for the synthesis of hexahydro-6H-benzo[c]chromenones and application
title_sort enantioselective organocatalytic domino michael-acetalization-henry reaction for the synthesis of hexahydro-6h-benzo[c]chromenones and application
publishDate 2015
url http://ndltd.ncl.edu.tw/handle/pfz88t
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AT xièyǔyòu enantioselectiveorganocatalyticdominomichaelacetalizationhenryreactionforthesynthesisofhexahydro6hbenzocchromenonesandapplication
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