[4+1] cyclization of α-diazo esters and mesoionic N-heterocyclic olefins-Reference-Cited by-同舟云学术

[4+1] cyclization of α-diazo esters and mesoionic N-heterocyclic olefins

Published:2023 Issue:32 Volume:59 Page:4770-4773
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Liang Qiuming¹²^ORCID,Zeng Yimin¹,Mendez Ocampo Pedro A.¹,Zhu Hui³,Qu Zheng-Wang³^ORCID,Grimme Stefan³^ORCID,Song Datong¹^ORCID

Affiliation:

1. Davenport Chemical Research Laboratories Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada

2. School of Science and Institute of Scientific Research, Great Bay University, Dongguan 523000, China

3. Mulliken Center for Theoretical Chemistry, University of Bonn, Beringstr. 4, Bonn 53115, Germany

Abstract

We report the reactivity of 1,2,3-trizole-derived mesoionic N-heterocyclic olefins toward α-diazoesters.

Funder

Natural Sciences and Engineering Research Council of Canada

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC01139A

Reference56 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. 1,3-Dipolar Cycloaddition Chemistry , ed. A. Padwa , Wiley , New York , vol. 1 & 2, 1984

3. In The Chemistry of Heterocyclic Compounds, Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products , ed. A. Padwa and W. H. Pearson , Wiley , New York , 2002 , vol. 59

4. H.Suga , K.Itoh , in Methods and Applications of Cycloaddition Reactions in Organic Syntheses , ed. N. Nishiwaki , Wiley , Hoboken , 2014 , chap. 7, pp. 175

5. The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pyridinium‐abgeleitete mesoionische N‐heterocyclische Olefine (py‐mNHOs);Angewandte Chemie;2024-01-18

2. Pyridinium‐Derived Mesoionic N‐Heterocyclic Olefins (py‐mNHOs);Angewandte Chemie International Edition;2024-01-18

3. A Facile Preparation of N‐Heterocyclic Olefins: Ring‐Opening Polymerization of β‐Butyrolactone and Frustrated Lewis Pair Reactivity**;Chemistry – A European Journal;2023-12-18

4. Pushing the Upper Limit of Nucleophilicity Scales by Mesoionic N‐Heterocyclic Olefins;Angewandte Chemie International Edition;2023-08-29

5. Mesoionische N‐Heterocyclische Olefine verschieben die obere Grenze der Nucleophilie‐Skala;Angewandte Chemie;2023-08-29