Asymmetric Synthesis of Chiral Aliphatic α-Tertiary Aminonitriles via Organocatalytic Isomerization of Cyanoketimines

IF 5.5 1区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ling Xu, Jisheng Luo, Li Deng
{"title":"Asymmetric Synthesis of Chiral Aliphatic α-Tertiary Aminonitriles via Organocatalytic Isomerization of Cyanoketimines","authors":"Ling Xu,&nbsp;Jisheng Luo,&nbsp;Li Deng","doi":"10.1002/cjoc.202400774","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Chiral <i>α</i>-tertiary aminonitriles are valuable synthetic intermediates. They are also found in various structures of biologically active molecules. Therefore, numerous reports of catalytic asymmetric synthesis of chiral <i>α</i>-aminonitriles continuously emerged during the past few decades. Great strides have been made for the synthesis of chiral <i>α</i>-aryl and <i>α</i>-branched alkyl aminonitriles. However, efficient methods for catalytic asymmetric synthesis of chiral <i>α</i>-linear alkyl aminonitriles remain limited. We herein report a new synthetic approach to chiral <i>α</i>-tertiary alkyl aminonitriles via catalytic asymmetric isomerization of cyanoketimines. The synthetic value of this method was illustrated by application to a concise catalytic asymmetric synthesis of vildagliptin.</p>\n <p>\n </p>\n </div>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"42 24","pages":"3387-3392"},"PeriodicalIF":5.5000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202400774","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Chiral α-tertiary aminonitriles are valuable synthetic intermediates. They are also found in various structures of biologically active molecules. Therefore, numerous reports of catalytic asymmetric synthesis of chiral α-aminonitriles continuously emerged during the past few decades. Great strides have been made for the synthesis of chiral α-aryl and α-branched alkyl aminonitriles. However, efficient methods for catalytic asymmetric synthesis of chiral α-linear alkyl aminonitriles remain limited. We herein report a new synthetic approach to chiral α-tertiary alkyl aminonitriles via catalytic asymmetric isomerization of cyanoketimines. The synthetic value of this method was illustrated by application to a concise catalytic asymmetric synthesis of vildagliptin.

通过氰基亚胺的有机催化异构化不对称合成手性脂肪族 α-叔氨基硝酸酯
手性 α-叔胺硝基化合物是非常有价值的合成中间体。它们还存在于各种生物活性分子结构中。因此,在过去几十年中,有关手性 α-氨基硝酸酯催化不对称合成的报道层出不穷。手性 α 芳基和 α 支链烷基氨腈的合成取得了长足进步。然而,催化不对称合成手性 α-线性烷基氨腈的有效方法仍然有限。我们在此报告一种通过氰基亚胺的催化不对称异构化合成手性 α-叔烷基氨腈的新方法。我们将这种方法应用于维达列汀的简便催化不对称合成,从而说明了它的合成价值。
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
Chinese Journal of Chemistry
Chinese Journal of Chemistry 化学-化学综合
CiteScore
8.80
自引率
14.80%
发文量
422
审稿时长
1.7 months
期刊介绍: The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.
×
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