The Intra- and Intermolecular Friedel-Crafts Acylation of Amino Acid Derivatives in Stereo-Retarded Manner

IF 1.7 3区 化学 Q3 CHEMISTRY, ORGANIC
Zetryana Puteri Tachrim, Makoto Hashimoto
{"title":"The Intra- and Intermolecular Friedel-Crafts Acylation of Amino Acid Derivatives in Stereo-Retarded Manner","authors":"Zetryana Puteri Tachrim, Makoto Hashimoto","doi":"10.2174/0113852728317263240510114622","DOIUrl":null,"url":null,"abstract":"\n\nThe Friedel-Crafts acylation of natural or unnatural amino acids in stereo-retarded manner is willing\nto prescribed here. Depending on its main skeleton, the typical intra- and intermolecular Friedel-Crafts reaction\nof amino acids can be differentiated. The unique amino acid’s general structure can contribute to the reaction\nbetween its carboxyl group and the side chain. Depending on the Friedel-Crafts reaction condition, the amino\nacid’s optical retention can be retarded. This perspective can contribute to the development of this one-century\nreaction in the field of organic chemistry.\n","PeriodicalId":10926,"journal":{"name":"Current Organic Chemistry","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/0113852728317263240510114622","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

The Friedel-Crafts acylation of natural or unnatural amino acids in stereo-retarded manner is willing to prescribed here. Depending on its main skeleton, the typical intra- and intermolecular Friedel-Crafts reaction of amino acids can be differentiated. The unique amino acid’s general structure can contribute to the reaction between its carboxyl group and the side chain. Depending on the Friedel-Crafts reaction condition, the amino acid’s optical retention can be retarded. This perspective can contribute to the development of this one-century reaction in the field of organic chemistry.
氨基酸衍生物的分子内和分子间Friedel-Crafts立体残基酰化反应
这里愿意介绍天然或非天然氨基酸的弗里德尔-卡夫酰化反应。根据氨基酸的主要骨架,可以区分典型的分子内和分子间 Friedel-Crafts 反应。独特的氨基酸总体结构有助于其羧基和侧链之间的反应。根据弗里德尔-卡夫斯反应条件的不同,氨基酸的光学保留时间也会不同。这一观点有助于这一百年反应在有机化学领域的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Current Organic Chemistry
Current Organic Chemistry 化学-有机化学
CiteScore
3.70
自引率
7.70%
发文量
76
审稿时长
1 months
期刊介绍: Current Organic Chemistry aims to provide in-depth/mini reviews on the current progress in various fields related to organic chemistry including bioorganic chemistry, organo-metallic chemistry, asymmetric synthesis, heterocyclic chemistry, natural product chemistry, catalytic and green chemistry, suitable aspects of medicinal chemistry and polymer chemistry, as well as analytical methods in organic chemistry. The frontier reviews provide the current state of knowledge in these fields and are written by chosen experts who are internationally known for their eminent research contributions. The Journal also accepts high quality research papers focusing on hot topics, highlights and letters besides thematic issues in these fields. Current Organic Chemistry should prove to be of great interest to organic chemists in academia and industry, who wish to keep abreast with recent developments in key fields of organic chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信