Deoxygenation of oximes for the synthesis of pyrrolines<i>via</i>hydroimination cyclization-Reference-Cited by-同舟云学术

Deoxygenation of oximes for the synthesis of pyrrolinesviahydroimination cyclization

Published:2023 Issue:16 Volume:21 Page:3350-3354
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Han Wencheng¹,Liu Wen-Deng¹,Su Junqi¹,Zhao Jiannan¹^ORCID

Affiliation:

1. Zhang Dayu School of Chemistry, Dalian University of Technology, Dalian 116024, P. R. China

Abstract

A series of pyrrolines were synthesizedviacyclization of iminyl radicals, which were generated by photocatalytic deoxygenation of oximes with trivalent phosphine.

Funder

Fundamental Research Funds for the Central Universities

Dalian University of Technology

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00072A

Reference63 articles.

1. Catalytic Radical Cyclization of Oximes Induced by One-Electron Transfer

2. Recent progress in the generation and use of nitrogen-centred radicals

3. The Oxime Portmanteau Motif: Released Heteroradicals Undergo Incisive EPR Interrogation and Deliver Diverse Heterocycles

4. Functionalised Oximes: Emergent Precursors for Carbon-, Nitrogen- and Oxygen-Centred Radicals

5. Visible light photoredox-controlled reactions of N-radicals and radical ions

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