| アイテムタイプ |
itemtype_ver1(1) |
| 公開日 |
2026-01-05 |
| タイトル |
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タイトル |
Synthesis of Diazatricyclic Molecules via Intramolecular Cycloaddition of Azomethine Ylides |
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言語 |
en |
| 著者 |
Kato, Satoru
Morita, Kaito
Umekubo, Nariyoshi
Yokoshima, Satoshi
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| アクセス権 |
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アクセス権 |
embargoed access |
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アクセス権URI |
http://purl.org/coar/access_right/c_f1cf |
| 権利 |
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|
権利情報 |
This document is the Accepted Manuscript version of a Published Work that appeared in final form in [ORGANIC LETTERS], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see [https://pubs.acs.org/articlesonrequest/AOR-V2YRHIZ8DDZPEGNBBRKM].” |
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言語 |
en |
| 内容記述 |
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内容記述タイプ |
Abstract |
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内容記述 |
Diazatricyclic molecules were synthesized via a modular approach. Starting from allylglycinol and amino acids, 2-ketopiperazines bearing an alkene unit were prepared. Upon heating with aldehydes, these 2-ketopiperazines generated azomethine ylides, which underwent intramolecular cycloaddition to construct the tricyclic core. The synthesis was completed in five or eight steps, with three or four substituents introduced in a modular fashion, respectively. |
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言語 |
en |
| 出版者 |
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出版者 |
ACS Publications |
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言語 |
en |
| 言語 |
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|
言語 |
eng |
| 資源タイプ |
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|
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 |
| 関連情報 |
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|
関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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|
関連識別子 |
https://doi.org/10.1021/acs.orglett.5c03537 |
| 収録物識別子 |
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収録物識別子タイプ |
PISSN |
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収録物識別子 |
1523-7060 |
| 書誌情報 |
en : ORGANIC LETTERS
巻 27,
号 38,
p. 10904-10907,
発行日 2025-09-26
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| ファイル公開日 |
|
|
日付 |
2026-09-26 |
|
日付タイプ |
Available |
kato_OL.pdf (538 KB)
