Pd-Catalyzed carboannulation of γ,δ-alkenyl oximes: efficient access to 5-membered cyclic nitrones and dihydroazines-Reference-Cited by-同舟云学术

Pd-Catalyzed carboannulation of γ,δ-alkenyl oximes: efficient access to 5-membered cyclic nitrones and dihydroazines

Published:2019 Issue:3 Volume:6 Page:388-392
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Sun Baozhen¹²³⁴⁵,Liu Shuang¹²³⁴⁵,Zhang Mengru¹²³⁴⁵,Zhao Jinbo¹²³⁴⁵^ORCID,Zhang Qian¹²³⁴⁵

Affiliation:

1. Jilin Province Key Laboratory of Functional Organic Molecule Design & Synthesis

2. Department of Chemistry

3. Northeast Normal University

4. Changchun

5. China

Abstract

The Pd⁰-catalyzed carboannulation of γ,δ-alkenyl oximes with organohalides offers catalyst-controlled access to 5-membered cyclic nitrones or 6-membered cyclic oxime ethers.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jilin Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C8QO01076E

Reference56 articles.

1. Polyalkoxy Nitrones as Chiral Building Blocks in Asymmetric Synthesis

2. Nitrones as therapeutics

3. Potential implication of the chemical properties and bioactivity of nitrone spin traps for therapeutics

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