Excellent enantioselective organocatalytic one-pot desymmetrization of meso-1,2-diols through asymmetric acylation and silylation by a chiral 1,2-diamine derived from (S)-proline

• 資料種別: 記事
• タイトル: Excellent enantioselective organocatalytic one-pot desymmetrization of meso-1,2-diols through asymmetric acylation and silylation by a chiral 1,2-diamine derived from (S)-proline
• 著者・編者: Hirofumi Nakayama; Hitomi Urai; Takeshi Oriyama
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-06-24
• 出版年（W3CDTF）: 2022-06-24
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(8)
• 掲載巻: 95(8)
• ISSN（掲載誌）: 1348-0634
• ISSN-L（掲載誌）: 0009-2673
• 本文の言語コード: eng
• DOI: 10.1246/bcsj.20220096; https://doi.org/10.1246/bcsj.20220096
• 国立国会図書館永続的識別子: info:ndljp/pid/12686447; https://dl.ndl.go.jp/pid/12686447
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会; https://dl.ndl.go.jp/collections/B00043
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2023-03-07T17:43:09+09:00
• 保存日（W3CDTF）: 2023-01-20
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://www.journal.csj.jp/toc/bcsj/95/8
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686446; https://dl.ndl.go.jp/pid/12686446
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
• DOI: 10.1246/bcsj.20220096; https://doi.org/10.1246/bcsj.20220096
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12686447; https://dl.ndl.go.jp/pid/12686447; https://academic.oup.com/bcsj/article-pdf/95/8/1217/56314158/bcsj.20220096.pdf
• 参照: Asymmetric desymmetrization of <i>meso</i>-diols by <i>C</i>₂-symmetric chiral 4-pyrrolidinopyridines; https://cir.nii.ac.jp/crid/1050282810757433344; Synthesis of the C(1)–C(13) Fragment of Leiodermatolide via Hydrogen-Mediated C–C Bond Formation; https://cir.nii.ac.jp/crid/1360016865823747072; Green Chemistry Meets Asymmetric Organocatalysis: A Critical Overview on Catalysts Synthesis; https://cir.nii.ac.jp/crid/1360016870096661888; Integrated Experimental and Computational Studies on the Organocatalytic Kinetic Resolution of β-Unfunctionalized Primary Alcohols Using a Chiral 1,2-Diamine: The Importance of Noncovalent Interactions; https://cir.nii.ac.jp/crid/1360298338450217088; Synthesis of (+)‐Darwinolide, a Biofilm‐Penetrating Anti‐MRSA Agent; https://cir.nii.ac.jp/crid/1360298343469276800; Desymmetrisation of meso-diols mediated by non-enzymatic acyl transfer catalysts; https://cir.nii.ac.jp/crid/1360574094969698304; Catalytic Asymmetrization of cis-2-Cyclopentene-1,4-diol. Highly Efficient and Practical Synthesis of (R)-4-Benzoyloxy-2-cyclopenten-1-one; https://cir.nii.ac.jp/crid/1360574095200835584; Asymmetric organocatalysis: an enabling technology for medicinal chemistry; https://cir.nii.ac.jp/crid/1360579818099342464; Enantioselective organocatalytic approaches to active pharmaceutical ingredients – selected industrial examples; https://cir.nii.ac.jp/crid/1360579818424230400; Organocatalysis: Trends of Drug Synthesis in Medicinal Chemistry; https://cir.nii.ac.jp/crid/1360579820250654080; Desymmetrization of <i>meso</i>-1,2-Diols by a Chiral <i>N</i>,<i>N</i>-4-Dimethylaminopyridine Derivative Containing a 1,1′-Binaphthyl Unit: Importance of the Hydroxy Groups; https://cir.nii.ac.jp/crid/1360846641538819968; Catalytic Asymmetric Acylation of Racemic Secondary Alcohols with Benzoyl Chloride in the Presence of a Chiral Diamine; https://cir.nii.ac.jp/crid/1360846644039777664; Highly Efficient and Enantioselective Method for the Synthesis of Chiral Building Blocks Derived from <i>meso</i>-1,3-Propanediols; https://cir.nii.ac.jp/crid/1360846644040249728; Organocatalysis: A Brief Overview on Its Evolution and Applications; https://cir.nii.ac.jp/crid/1360855571307955840; Asymmetric Desymmetrization of <i>meso</i>‐1,2‐Diols by Phosphinite Derivatives of Cinchona Alkaloids; https://cir.nii.ac.jp/crid/1361137045530249344; Remarkably Fast Acylation of Alcohols with Benzoyl Chloride Promoted by TMEDA; https://cir.nii.ac.jp/crid/1361418520169032832; Enantioselective silyl protection of alcohols catalysed by an amino-acid-based small molecule; https://cir.nii.ac.jp/crid/1361981468506688256; Organocatalytic kinetic resolution of racemic primary alcohols using a chiral 1,2-diamine derived from (S)-proline; https://cir.nii.ac.jp/crid/1361981469940668032; The advent and development of organocatalysis; https://cir.nii.ac.jp/crid/1361981470882175104; Asymmetric Aminocatalysis—Gold Rush in Organic Chemistry; https://cir.nii.ac.jp/crid/1362262944088957696; Enantioselective silyl protection of alcohols promoted by a combination of chiral and achiral Lewis basic catalysts; https://cir.nii.ac.jp/crid/1362262945376992000; Organocatalyzed Enantioselective Desymmetrization of Diols in the Preparation of Chiral Building Blocks; https://cir.nii.ac.jp/crid/1362544419273341312; Introduction: Organocatalysis; https://cir.nii.ac.jp/crid/1362825895197042560; Highly efficient catalytic asymmetric acylation of meso-1,2-diols with benzoyl chloride in the presence of a chirai diamine combined with Et3N; https://cir.nii.ac.jp/crid/1363107368934565248; Asymmetric synthesis of sceletium alkaloids: (−)-mesembrine, (+)-sceletium A-4, (+)-tortuosamine and (+)-N-formyltortuosamine; https://cir.nii.ac.jp/crid/1363107369240403456; Organocatalytic enantioselective desymmetrisation; https://cir.nii.ac.jp/crid/1363388844848999296; Recent topics in the desymmetrization of meso-diols; https://cir.nii.ac.jp/crid/1363670318784454528; Scaffolding Catalysts: Highly Enantioselective Desymmetrization Reactions; https://cir.nii.ac.jp/crid/1363670319707478784; Truncated Cinchona alkaloids as catalysts in enantioselective monobenzoylation of meso-1,2-diols; https://cir.nii.ac.jp/crid/1364233268761796736; Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains; https://cir.nii.ac.jp/crid/1364233270645220992
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 12686447; http://id.ndl.go.jp/bib/12686447