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Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones

A novel and efficient rearrangement of N-tosylhydrazones bearing allyl ethers into trans-olefin-substituted sulfonylhydrazones is proposed. The reaction involves breakage of the C-O bond and formation of the C-N bond. The reaction can be extended to a wide range of substrates, and the target product...

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Autores principales: Chang, Yaoyao, Fu, Jianfang, Li, Yingxue, Ding, Rongcai, Liu, Yue, Hu, Jinxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573317/
https://www.ncbi.nlm.nih.gov/pubmed/34760873
http://dx.doi.org/10.3389/fchem.2021.782641
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author Chang, Yaoyao
Fu, Jianfang
Li, Yingxue
Ding, Rongcai
Liu, Yue
Hu, Jinxing
author_facet Chang, Yaoyao
Fu, Jianfang
Li, Yingxue
Ding, Rongcai
Liu, Yue
Hu, Jinxing
author_sort Chang, Yaoyao
collection PubMed
description A novel and efficient rearrangement of N-tosylhydrazones bearing allyl ethers into trans-olefin-substituted sulfonylhydrazones is proposed. The reaction involves breakage of the C-O bond and formation of the C-N bond. The reaction can be extended to a wide range of substrates, and the target products can be synthesized smoothly, regardless of the presence of electron-donating and electron-withdrawing groups. The proposed strategy is a new direction in the field of rearrangement reactions.
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spelling pubmed-85733172021-11-09 Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones Chang, Yaoyao Fu, Jianfang Li, Yingxue Ding, Rongcai Liu, Yue Hu, Jinxing Front Chem Chemistry A novel and efficient rearrangement of N-tosylhydrazones bearing allyl ethers into trans-olefin-substituted sulfonylhydrazones is proposed. The reaction involves breakage of the C-O bond and formation of the C-N bond. The reaction can be extended to a wide range of substrates, and the target products can be synthesized smoothly, regardless of the presence of electron-donating and electron-withdrawing groups. The proposed strategy is a new direction in the field of rearrangement reactions. Frontiers Media S.A. 2021-10-25 /pmc/articles/PMC8573317/ /pubmed/34760873 http://dx.doi.org/10.3389/fchem.2021.782641 Text en Copyright © 2021 Chang, Fu, Li, Ding, Liu and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Chang, Yaoyao
Fu, Jianfang
Li, Yingxue
Ding, Rongcai
Liu, Yue
Hu, Jinxing
Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title_full Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title_fullStr Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title_full_unstemmed Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title_short Pd-Catalyzed Rearrangement Reaction of N-Tosylhydrazones Bearing Allyl Ethers Into Trans-Olefin-Substituted Sulfonylhydrazones
title_sort pd-catalyzed rearrangement reaction of n-tosylhydrazones bearing allyl ethers into trans-olefin-substituted sulfonylhydrazones
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573317/
https://www.ncbi.nlm.nih.gov/pubmed/34760873
http://dx.doi.org/10.3389/fchem.2021.782641
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