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Regioselective Introduction of Electrophiles into Piperidine Derivatives at the 4-Position
http://hdl.handle.net/10069/21989
http://hdl.handle.net/10069/219897b79d606-636e-4de2-9c43-cb970e103a9a
名前 / ファイル | ライセンス | アクション |
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Heterocycles76_177.pdf (137.8 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2009-06-16 | |||||
タイトル | ||||||
タイトル | Regioselective Introduction of Electrophiles into Piperidine Derivatives at the 4-Position | |||||
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 |
Onomura, Osamu
× Onomura, Osamu× Fujimura, Noriyuki× Oda, Takahisa× Matsumura, Yoshihiro× Demizu, Yosuke |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Regioselective introduction of various electrophiles (aldehydes, ketones, and imines) into piperidine skeleton at the 4-position was achieved with a catalytic amount of Pd(OAc)2/PPh3 in the presence of excess Et2Zn. In addition, enantioselective introduction of benzaldehyde into piperidine derivatives was accomplished by using chiral phosphine ligand with moderate enantioselectivity. | |||||
書誌情報 |
HETEROCYCLES 巻 76, 号 1, p. 177-182, 発行日 2008-09 |
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出版者 | ||||||
出版者 | Japan Institute of Heterocyclic Chemistry | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 03855414 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00663739 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.3987/COM-08-S(N)26 | |||||
権利 | ||||||
権利情報 | Copyright c 2008 The Japan Institute of Heterocyclic Chemistry | |||||
著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Heterocycles, 76(1), pp.177-182; 2008 |