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標(biāo)題: Titlebook: Discrimination of Mobile Supramolecular Chirality; Acylative Molecular Ayumi Imayoshi Book 2022 Springer Nature Singapore Pte Ltd. 2022 As [打印本頁(yè)]

作者: 筆記    時(shí)間: 2025-3-21 17:13
書(shū)目名稱(chēng)Discrimination of Mobile Supramolecular Chirality影響因子(影響力)




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作者: 嬰兒    時(shí)間: 2025-3-21 20:17

作者: 兇兆    時(shí)間: 2025-3-22 00:38
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.?.).
作者: 無(wú)能性    時(shí)間: 2025-3-22 07:30
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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作者: Gustatory    時(shí)間: 2025-3-24 00:41
https://doi.org/10.1007/978-3-030-16985-5stigated the monoacylation of 1,5-pentanediol (.) in the presence of .-symmetric catalysts .–.. The amide carbonyl group of the catalysts was suggested to play a main role for the selective monoacylation of .. The indolyl NH groups in the side chains of the catalysts seem to also contribute to incre
作者: 思考    時(shí)間: 2025-3-24 05:16
Luís Renato Vedovato,Cristiane G. F. Vianna . afforded a mechanically planar chiral rotaxane . with perfect enantiopurity (>99% ee) in 29% yield (the theoretical maximum yield of kinetic resolution of racemate is 50%) (Fig.?.). The catalysts enabled to discriminate mobile mechanical chirality of the rotaxanes with the excellent selectivity i
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作者: 震驚    時(shí)間: 2025-3-25 09:41
Luís Renato Vedovato,Cristiane G. F. Viannaill stand as unsolved problems. Supramolecules such as rotaxanes and catenanes are known to possess mechanical chirality when each of the axis and/or ring components has dissymmetry (Fig.?.) (Frisch and Wasserman in J Am Chem Soc 83:3789–3795, 1961, [.]; Schill in Catenanes, rotaxanes and knots, Aca
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作者: reject    時(shí)間: 2025-3-25 18:11

作者: Ordeal    時(shí)間: 2025-3-25 21:18
https://doi.org/10.1007/978-981-16-7431-0Asymmetric synthesis; Synthesis of chiral supramolecules; Rotaxane; Molecular transformations; Molecular
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作者: 惡意    時(shí)間: 2025-3-26 13:27
Springer Theseshttp://image.papertrans.cn/e/image/281225.jpg
作者: expdient    時(shí)間: 2025-3-26 20:42
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