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  1. D400 創薬科学研究科
  2. D400a 雑誌掲載論文
  3. 学術雑誌

Total Synthesis of Lycoposerramine-R

http://hdl.handle.net/2237/00029249
http://hdl.handle.net/2237/00029249
dcc22a22-c66e-4055-9bfd-c9ef529d7dee
名前 / ファイル ライセンス アクション
20180831_watanabe.pdf 20180831_watanabe (301.2 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2019-02-06
タイトル
タイトル Total Synthesis of Lycoposerramine-R
言語 en
著者 Watanabe, Shinya

× Watanabe, Shinya

WEKO 88608

en Watanabe, Shinya

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Ishikawa, Masatsugu

× Ishikawa, Masatsugu

WEKO 88609

en Ishikawa, Masatsugu

Search repository
Nomura, Toshimune

× Nomura, Toshimune

WEKO 88610

en Nomura, Toshimune

Search repository
Fukuyama, Tohru

× Fukuyama, Tohru

WEKO 88611

en Fukuyama, Tohru

Search repository
Yokoshima, Satoshi

× Yokoshima, Satoshi

WEKO 88612

en Yokoshima, Satoshi

Search repository
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
キーワード
主題Scheme Other
主題 alkaloids
キーワード
主題Scheme Other
主題 Diels–Alder reaction
キーワード
主題Scheme Other
主題 total synthesis
キーワード
主題Scheme Other
主題 gold catalysis
キーワード
主題Scheme Other
主題 alkaloids
キーワード
主題Scheme Other
主題 rearrangement
抄録
内容記述 A total synthesis of lycoposerramine-R was accomplished. The synthesis featured a Claisen–Ireland rearrangement to install a two-carbon unit, and a hetero-Diels–Alder reaction to form a cyclic enol ether that reacted with an ethynyl group to construct a cis-hydrindane core containing a quaternary carbon. A 2-pyridone synthesis using 2-(phenylsulfinyl)acetamide was used to complete the synthesis.
言語 en
内容記述タイプ Abstract
内容記述
内容記述 ファイル公開:2019-11-01
言語 ja
内容記述タイプ Other
出版者
言語 en
出版者 Georg Thieme Verlag
言語
言語 eng
資源タイプ
資源タイプresource http://purl.org/coar/resource_type/c_6501
タイプ journal article
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1055/s-0037-1611024
ISSN(print)
収録物識別子タイプ PISSN
収録物識別子 0936-5214
書誌情報 en : Synlett

巻 29, 号 18, p. 2377-2380, 発行日 2018-11
著者版フラグ
値 author
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