找回密码
 To register

QQ登录

只需一步,快速开始

扫一扫,访问微社区

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

[复制链接]
查看: 8080|回复: 36
发表于 2025-3-21 17:13:40 | 显示全部楼层 |阅读模式
书目名称Discrimination of Mobile Supramolecular Chirality
副标题Acylative Molecular
编辑Ayumi Imayoshi
视频video
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
丛书名称Springer Theses
图书封面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
关键词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

书目名称Discrimination of Mobile Supramolecular Chirality影响因子(影响力)




书目名称Discrimination of Mobile Supramolecular Chirality影响因子(影响力)学科排名




书目名称Discrimination of Mobile Supramolecular Chirality网络公开度




书目名称Discrimination of Mobile Supramolecular Chirality网络公开度学科排名




书目名称Discrimination of Mobile Supramolecular Chirality被引频次




书目名称Discrimination of Mobile Supramolecular Chirality被引频次学科排名




书目名称Discrimination of Mobile Supramolecular Chirality年度引用




书目名称Discrimination of Mobile Supramolecular Chirality年度引用学科排名




书目名称Discrimination of Mobile Supramolecular Chirality读者反馈




书目名称Discrimination of Mobile Supramolecular Chirality读者反馈学科排名




单选投票, 共有 0 人参与投票
 

0票 0%

Perfect with Aesthetics

 

0票 0%

Better Implies Difficulty

 

0票 0%

Good and Satisfactory

 

0票 0%

Adverse Performance

 

0票 0%

Disdainful Garbage

您所在的用户组没有投票权限
发表于 2025-3-21 20:17:32 | 显示全部楼层
发表于 2025-3-22 00:38:42 | 显示全部楼层
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. .).
发表于 2025-3-22 07:30:03 | 显示全部楼层
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.
发表于 2025-3-22 09:32:02 | 显示全部楼层
发表于 2025-3-22 13:49:11 | 显示全部楼层
发表于 2025-3-22 19:52:09 | 显示全部楼层
发表于 2025-3-22 22:51:28 | 显示全部楼层
发表于 2025-3-23 01:32:36 | 显示全部楼层
发表于 2025-3-23 07:09:42 | 显示全部楼层
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,
 关于派博传思  派博传思旗下网站  友情链接
派博传思介绍 公司地理位置 论文服务流程 影响因子官网 SITEMAP 大讲堂 北京大学 Oxford Uni. Harvard Uni.
发展历史沿革 期刊点评 投稿经验总结 SCIENCEGARD IMPACTFACTOR 派博系数 清华大学 Yale Uni. Stanford Uni.
|Archiver|手机版|小黑屋| 派博传思国际 ( 京公网安备110108008328) GMT+8, 2025-5-4 00:49
Copyright © 2001-2015 派博传思   京公网安备110108008328 版权所有 All rights reserved
快速回复 返回顶部 返回列表