Palladium-catalyzed allylic alkylation of hydrazones with hydroxy-tethered allyl carbonates: synthesis of functionalized hydrazones-Reference-Cited by-同舟云学术

Palladium-catalyzed allylic alkylation of hydrazones with hydroxy-tethered allyl carbonates: synthesis of functionalized hydrazones

Published:2022 Issue:21 Volume:9 Page:5851-5857
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xu Jiaqing¹,Liu Min¹,Hu Yimin¹^ORCID,Wang Lei²,Wang Wei³,Wu Yongjun³,Guo Hongchao¹^ORCID

Affiliation:

1. Department of Chemistry, Innovation Center of Pesticide Research, and Department of Nutrition and Health, China Agricultural University, Beijing 100193, P. R. China

2. Nutrichem, Co., LTD, Beijing, China

3. College of Public Health, Zhengzhou University, Zhengzhou 450001, P. R. China

Abstract

Pd-catalyzed allylic alkylation of hydroxy-tethered allyl carbonates and hydrazones worked well without an external base to afford various E configurations of functionalized hydrazones, which were successfully transformed into pyridazines.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO01186G

Reference48 articles.

1. A review exploring biological activities of hydrazones

2. The bioactivity of benzenesulfonyl hydrazones: A short review

3. Palladium-Catalyzed Allylic Alkylation Using Chiral Hydrazones as Ligands

4. Palladium-catalyzed asymmetric allylic alkylation using chiral hydrazone ligands with ferrocene skeleton

5. Phosphine-Free Hydrazone−Pd Complex as the Catalyst Precursor for a Suzuki−Miyaura Reaction under Mild Aerobic Conditions

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