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| ファイル | 記述 | サイズ | フォーマット | |
|---|---|---|---|---|
| s-0036-1588141.pdf | 427.69 kB | Adobe PDF | 見る/開く |
| タイトル: | Enantioselective Synthesis of anti-β-Hydroxy-α-amino Esters via an Organocatalyzed Decarboxylative Aldol Reaction |
| 著者: | Takemoto, Yoshiji    https://orcid.org/0000-0003-1375-3821 (unconfirmed)March, Taryn Murata, Akihiro Kobayashi, Yusuke https://orcid.org/0000-0003-3074-7378 (unconfirmed) |
| 著者名の別形: | 竹本, 佳司 小林, 祐輔 |
| キーワード: | bifunctional organocatalyst cinchona alkaloid malonic acid half oxyester (MAHO) sulfonamide β-hydroxy-α-amino acid |
| 発行日: | Jul-2017 |
| 出版者: | Georg Thieme Verlag |
| 誌名: | Synlett |
| 巻: | 28 |
| 号: | 11 |
| 開始ページ: | 1295 |
| 終了ページ: | 1299 |
| 抄録: | The first enantioselective decarboxylative aldol addition with α-amido-substituted malonic acid half oxyesters (MAHOs) is described. The combined use of a newly designed bifunctional sulfonamide catalyst with pentafluorobenzoic acid as an additive afforded the β-hydroxy-α-amino acid derivatives in moderate to high yields and with high enantioselectivities. |
| 著作権等: | This is the accepted manuscript of the article, which has been published in final form at http://doi.org/10.1055/s-0036-1588141 The full-text file will be made open to the public on 2 March 2018 in accordance with publisher's 'Terms and Conditions for Self-Archiving'. This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。 |
| URI: | http://hdl.handle.net/2433/243148 |
| DOI(出版社版): | 10.1055/s-0036-1588141 |
| 出現コレクション: | 学術雑誌掲載論文等 |
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