Iron-catalyzed oxidative cyclization of olefinic 1,3-dicarbonyls with ketone C(sp3)–H bonds: facile access to 2,3-dihydrofurans-Reference-Cited by-同舟云学术

Iron-catalyzed oxidative cyclization of olefinic 1,3-dicarbonyls with ketone C(sp3)–H bonds: facile access to 2,3-dihydrofurans

Published:2021 Issue:30 Volume:45 Page:13639-13643
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kang Qing-Qing¹²³⁴⁵,Meng Ya-Nan¹²³⁴⁵,Zhang Jun-Hao¹²³⁴⁵,Li Long¹²³⁴⁵,Ge Guo-Ping¹²³⁴⁵,Zheng Hongxing⁶⁷⁸⁹¹⁰,Liu Hongxin¹¹¹²¹³¹⁴¹⁰^ORCID,Wei Wen-Ting¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Advanced Mass Spectrometry and Molecular Analysis of Zhejiang Province

2. State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products

3. School of Materials Science and Chemical Engineering

4. Ningbo University

5. Ningbo

6. Institution of Functional Organic Molecules and Materials

7. School of Chemistry and Chemical Engineering

8. Liaocheng University

9. Liaocheng

10. China

11. College of Chemistry and Materials Engineering

12. Institute of New Materials & Industrial Technology

13. Wenzhou University

14. Wenzhou

Abstract

The reaction involves the addition of an α-carbonyl radical to the CC bond of olefinic 1,3-dicarbonyls followed by intramolecular 5-endo-trig cyclization.

Funder

The Fundamental Research Funds for the Provincial Universities of Zhejiang

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/NJ/D1NJ02378K

Reference72 articles.

1. Iron‐Catalyzed Cross‐Couplings in the Synthesis of Pharmaceuticals: In Pursuit of Sustainability