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Highly enantioselective reaction of lithiated N-Boc-thiazolidine: A new chiral formyl anion equivalent
https://nitech.repo.nii.ac.jp/records/5205
https://nitech.repo.nii.ac.jp/records/52055b0834e5-fd9a-4f52-bbab-8282f02f8527
名前 / ファイル | ライセンス | アクション |
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本文_fulltext (308.8 kB)
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Org. Biomol. Chem . , 2004, 2, 2168-2169 -Reproduced by permission of The Royal Society of Chemistry (RSC)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2012-11-06 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Highly enantioselective reaction of lithiated N-Boc-thiazolidine: A new chiral formyl anion equivalent | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Wang, Libo
× Wang, Libo× Nakamura, Shuichi× Toru, Takeshi |
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著者別名 | ||||||
姓名 | 中村, 修一 | |||||
著者別名 | ||||||
姓名 | 融, 健 | |||||
書誌情報 |
Organic & biomolecular chemistry 巻 2, 号 15, p. 2168-2169, 発行日 2004-07-08 |
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出版者 | ||||||
出版者 | Royal Society of Chemistry | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 14770520 | |||||
書誌レコードID(NCID) | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA1168650X | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | http://dx.doi.org/10.1039/b408509d | |||||
関連名称 | 10.1039/b408509d | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Reaction of lithiated N-Boc-thiazolidine 1 with various aldehydes in the presence of (-)-sparteine afforded the products with up to 93% ee. The reaction was confirmed to proceed through a dynamic thermodynamic resolution pathway. Each diastereomeric alcohol could be converted to the corresponding optically active 1,2-ethanediols. | |||||
フォーマット | ||||||
内容記述タイプ | Other | |||||
内容記述 | application/pdf |