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Titlebook: Discrimination of Mobile Supramolecular Chirality; Acylative Molecular Ayumi Imayoshi Book 2022 Springer Nature Singapore Pte Ltd. 2022 As

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發(fā)表于 2025-3-21 17:13:40 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Discrimination of Mobile Supramolecular Chirality
副標(biāo)題Acylative Molecular
編輯Ayumi Imayoshi
視頻videohttp://file.papertrans.cn/282/281225/281225.mp4
概述Nominated by Kyoto University as an outstanding Ph.D. thesis.Presents a detailed description and a variety of examples of molecular transformations.Enables understanding of qualitatively novel asymmet
叢書(shū)名稱Springer Theses
圖書(shū)封面Titlebook: Discrimination of Mobile Supramolecular Chirality; Acylative Molecular  Ayumi Imayoshi Book 2022 Springer Nature Singapore Pte Ltd. 2022 As
描述This book proposes a novel concept for molecular recognition. In the field of asymmetric synthesis approaching the mature science, asymmetric discrimination and catalytic synthesis of chiral supramolecules still stand as unsolved problems. The extreme difficulty in asymmetric synthesis of such supramolecules may result from the mobile nature of supramolecular chirality. Here the author shows the first highly enantioselective synthesis of mechanically chiral supramolecules. In the presence of a chiral organocatalyst, a mechanically planar chiral rotaxane was obtained with p erfect enantiopurity (>99% ee) with an excellent selectivity. The dynamic and flexible recognition mode enabled asymmetric synthesis of supramolecules with conformational flexibility and mobility. The recognition mode of the catalyst is a contrast to the traditional static and rigid recognition mode of the typical conventional catalysts. The concept of dynamic molecular recognition will be adopted as a novelconcept in a wide range of fields beyond the field of organic chemistry, including material chemistry, biochemistry, and medicinal chemistry..
出版日期Book 2022
關(guān)鍵詞Asymmetric synthesis; Synthesis of chiral supramolecules; Rotaxane; Molecular transformations; Molecular
版次1
doihttps://doi.org/10.1007/978-981-16-7431-0
isbn_softcover978-981-16-7433-4
isbn_ebook978-981-16-7431-0Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightSpringer Nature Singapore Pte Ltd. 2022
The information of publication is updating

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Appendix, resolution of rotaxanes (Chap. ., Fig.?.), only a small amount of catalytically active species (i.e., acylpyridinium salts) was actually produced. In this chapter, I investigated the efficiency of the formation of the acylpyridinium salts depending on the acyl donor in detail (Fig.?.).
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Conclusion and Perspectives,complex reaches the particular productive recognition mode. The dynamic and flexible recognition mode of the chiral PPY catalysts enabled discrimination of mobile and kinetic labile supramolecular chirality.
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Mechanistic Study of Organocatalytic Chemoselective Monoacylation of 1,5-Pentanediol,cular transformations of polyol compounds by using C.-symmetric chiral 4-pyrrolidinopyridine (PPY) catalysts bearing substrate-recognition sites consisting of amino acid side chains (Yoshida et al. in Angew Chem-Int Edn 50:4888–4892, 2011, [.]; Kawabata et al. in J Am Chem Soc 129:12890–12895, 2007,
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