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  1. B200 工学部/工学研究科
  2. B200a 雑誌掲載論文
  3. 学術雑誌

The Latest Insights into Multiply Selective Diels–Alder Reactions Using a Chiral‐Cavity‐Structured Lewis‐Acidic Boron Catalyst

http://hdl.handle.net/2237/0002012763
http://hdl.handle.net/2237/0002012763
9984d7d3-b396-4b9a-bfbb-2bc42b372972
名前 / ファイル ライセンス アクション
Manuscript.pdf Manuscript.pdf (8.5 MB)
アイテムタイプ itemtype_ver1(1)
公開日 2025-05-19
タイトル
タイトル The Latest Insights into Multiply Selective Diels–Alder Reactions Using a Chiral‐Cavity‐Structured Lewis‐Acidic Boron Catalyst
言語 en
著者 Matsui, Kai

× Matsui, Kai

en Matsui, Kai

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Toh, Kohei

× Toh, Kohei

en Toh, Kohei

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Sakamoto, Tatsuhiro

× Sakamoto, Tatsuhiro

en Sakamoto, Tatsuhiro

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Hatano, Manabu

× Hatano, Manabu

en Hatano, Manabu

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Ishihara, Kazuaki

× Ishihara, Kazuaki

en Ishihara, Kazuaki

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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
権利
権利情報 This is the peer reviewed version of the following article: [K. Matsui, K. Toh, T. Sakamoto, M. Hatano, K. Ishihara, Adv. Synth. Catal. 2025, 367, e202401560. https://doi.org/10.1002/adsc.202401560], which has been published in final form at [https://doi.org/10.1002/adsc.202401560]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited."
言語 en
内容記述
内容記述タイプ Abstract
内容記述 The latest insights into multiply selective Diels–Alder (DA) reactions is presented, where a chiral-cavity-structured Lewis-acidic boron catalyst is employed. The catalyst ((R)-1) is capable of recognizing both dienes and dienophiles, primarily due to the influence of the suitable steric factors of its cavity. By taking advantage of the structural and exo-product-inducing properties of (R)-1, even in the presence of a mixture of inseparable dienes, the target products were successfully obtained in high yield with high enantioselectivity. As (R)-1 exhibited the capacity to differentiate between three-dimensional isomeric transition-state structures in DA reactions, this work contributes to the advancement of artificial enzyme-like catalysis, which has so far remained elusive.
言語 en
出版者
出版者 Wiley
言語 en
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
関連情報
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1002/adsc.202401560
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 1615-4150
書誌情報 en : Advanced Synthesis & Catalysis

巻 367, 号 5, p. e202401560, 発行日 2025-03-04
ファイル公開日
日付 2026-03-04
日付タイプ Available
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