铑催化碳插入法对映选择性合成无环季碳

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Kun He, Weikun Zeng, Yingcheng Wang, Zhihui Shao, Yi Jin
{"title":"铑催化碳插入法对映选择性合成无环季碳","authors":"Kun He, Weikun Zeng, Yingcheng Wang, Zhihui Shao, Yi Jin","doi":"10.1021/acscatal.5c00841","DOIUrl":null,"url":null,"abstract":"Herein, the construction of acyclic quaternary carbon chiral centers through carbene insertions in a chiral metal carbene mechanism is reported. Carbene insertion products can be obtained with high chemical selectivity, regioselectivity, <i>Z/E</i> selectivity, and enantioselectivity using α-diazo esters and enone-hydrazones under the conditions of a chiral dirhodium catalyst. The mechanism verification experiments demonstrate that the benzene ring, originating from the enone-hydrazones, can shield the O and NH coordination atoms of the enone-hydrazones. This shielding effect is crucial for the asymmetric C–C bond insertion reaction catalyzed by a chiral metal carbene complex derived from a chiral dirhodium. Additionally, the results of the controlled experiments indicate that achieving the asymmetric version of the traditional C–C insertion substrate is challenging. This challenge arises from the coordination of the substrate with the Rh1 site of the chiral dirhodium catalyst, which subsequently leads to carbene precursor activation occurring at the Rh2 site, resulting in poor stereoselectivity.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"69 1","pages":""},"PeriodicalIF":13.1000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rh-Catalyzed Enantioselective Synthesis of Acyclic Quaternary Carbons via Carbene Insertion\",\"authors\":\"Kun He, Weikun Zeng, Yingcheng Wang, Zhihui Shao, Yi Jin\",\"doi\":\"10.1021/acscatal.5c00841\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, the construction of acyclic quaternary carbon chiral centers through carbene insertions in a chiral metal carbene mechanism is reported. Carbene insertion products can be obtained with high chemical selectivity, regioselectivity, <i>Z/E</i> selectivity, and enantioselectivity using α-diazo esters and enone-hydrazones under the conditions of a chiral dirhodium catalyst. The mechanism verification experiments demonstrate that the benzene ring, originating from the enone-hydrazones, can shield the O and NH coordination atoms of the enone-hydrazones. This shielding effect is crucial for the asymmetric C–C bond insertion reaction catalyzed by a chiral metal carbene complex derived from a chiral dirhodium. Additionally, the results of the controlled experiments indicate that achieving the asymmetric version of the traditional C–C insertion substrate is challenging. This challenge arises from the coordination of the substrate with the Rh1 site of the chiral dirhodium catalyst, which subsequently leads to carbene precursor activation occurring at the Rh2 site, resulting in poor stereoselectivity.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"69 1\",\"pages\":\"\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-03-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.5c00841\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.5c00841","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

本文报道了一种手性金属卡宾机理中通过卡宾插入构建无环季碳手性中心的方法。以α-重氮酯和烯酮腙为原料,在手性重钠催化剂的作用下,得到的插入产物具有较高的化学选择性、区域选择性、Z/E选择性和对映选择性。机理验证实验表明,源自于烯酮腙的苯环可以屏蔽烯酮腙的O和NH配位原子。这种屏蔽效应对于由手性钯衍生的手性金属卡宾配合物催化的不对称C-C键插入反应至关重要。此外,对照实验结果表明,实现传统C-C插入衬底的不对称版本是具有挑战性的。这一挑战来自于底物与手性钯催化剂的Rh1位点的配位,这随后导致在Rh2位点发生的碳前体活化,导致立体选择性差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rh-Catalyzed Enantioselective Synthesis of Acyclic Quaternary Carbons via Carbene Insertion

Rh-Catalyzed Enantioselective Synthesis of Acyclic Quaternary Carbons via Carbene Insertion
Herein, the construction of acyclic quaternary carbon chiral centers through carbene insertions in a chiral metal carbene mechanism is reported. Carbene insertion products can be obtained with high chemical selectivity, regioselectivity, Z/E selectivity, and enantioselectivity using α-diazo esters and enone-hydrazones under the conditions of a chiral dirhodium catalyst. The mechanism verification experiments demonstrate that the benzene ring, originating from the enone-hydrazones, can shield the O and NH coordination atoms of the enone-hydrazones. This shielding effect is crucial for the asymmetric C–C bond insertion reaction catalyzed by a chiral metal carbene complex derived from a chiral dirhodium. Additionally, the results of the controlled experiments indicate that achieving the asymmetric version of the traditional C–C insertion substrate is challenging. This challenge arises from the coordination of the substrate with the Rh1 site of the chiral dirhodium catalyst, which subsequently leads to carbene precursor activation occurring at the Rh2 site, resulting in poor stereoselectivity.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
×
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:604180095
Book学术官方微信