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Titlebook: Chemoselective Nucleophilic α-Amination of Amides; Miran Lemmerer Book 2020 The Editor(s) (if applicable) and The Author(s), under exclusi

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發(fā)表于 2025-3-21 16:30:14 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Chemoselective Nucleophilic α-Amination of Amides
編輯Miran Lemmerer
視頻videohttp://file.papertrans.cn/225/224935/224935.mp4
概述Organic Synthesis via Umpolung and Rearrangement
叢書名稱BestMasters
圖書封面Titlebook: Chemoselective Nucleophilic α-Amination of Amides;  Miran Lemmerer Book 2020 The Editor(s) (if applicable) and The Author(s), under exclusi
描述.α-Amino carbonyl compounds are omnipresent in all living organisms, making their selective synthesis highly sought after. However, the synthesis of α-amino amides, a subclass of α-amino carbonyls, in the presence of other carbonyls is usually challenging, due to the required harsh conditions. Miran Lemmerer expands a novel chemoselective approach for the synthesis of these intriguing molecules together with Univ.-Prof. Dr. Nuno Maulide’s team...The Author:.Miran Lemmerer. is currently pursuing his PhD studies under supervision of Prof. Dr. Nuno Maulide at the Department of Organic Chemistry, University of Vienna, Austria.?.
出版日期Book 2020
關(guān)鍵詞α-Amination; Organic Chemistry; Amide; Electrophilic Amide Activation; Amine; Umpolung Reaction; Chemosele
版次1
doihttps://doi.org/10.1007/978-3-658-30020-3
isbn_softcover978-3-658-30019-7
isbn_ebook978-3-658-30020-3Series ISSN 2625-3577 Series E-ISSN 2625-3615
issn_series 2625-3577
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Fachmedien Wies
The information of publication is updating

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Book 2020 Lemmerer expands a novel chemoselective approach for the synthesis of these intriguing molecules together with Univ.-Prof. Dr. Nuno Maulide’s team...The Author:.Miran Lemmerer. is currently pursuing his PhD studies under supervision of Prof. Dr. Nuno Maulide at the Department of Organic Chemistry, University of Vienna, Austria.?.
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發(fā)表于 2025-3-22 05:23:07 | 只看該作者
Book 2020-amino amides, a subclass of α-amino carbonyls, in the presence of other carbonyls is usually challenging, due to the required harsh conditions. Miran Lemmerer expands a novel chemoselective approach for the synthesis of these intriguing molecules together with Univ.-Prof. Dr. Nuno Maulide’s team...
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Chemoselective Nucleophilic α-Amination of Amides978-3-658-30020-3Series ISSN 2625-3577 Series E-ISSN 2625-3615
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Limit Cycles and Structural Stability,tion aldehydes, ketones, esters, amides and nitriles form enolates which react with electrophiles to yield α-functionalized products. Examples of such electrophiles include aldehydes, ketones or esters themselves.
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