Regiospecific Alkene Oxyamination via N‐Alkylation‐ Hydroxylation‐Transesterification Cascades.

Bibliographic Details
Title: Regiospecific Alkene Oxyamination via N‐Alkylation‐ Hydroxylation‐Transesterification Cascades.
Authors: Zhang, Hong‐Xia1 (AUTHOR), Kou, Li‐Gang1 (AUTHOR), Gao, Ya‐Ru1 (AUTHOR), Jia, Qiong1 (AUTHOR), Wang, Yong‐Qiang1 (AUTHOR) wangyq@nwu.edu.cn
Source: Advanced Synthesis & Catalysis. 3/18/2025, Vol. 367 Issue 6, p1-5. 5p.
Abstract: An unprecedented cascade reaction of simple inactive alkenes, azo compounds and H2O to produce valuable poly‐substituted oxazolidinones is reported herein. The transformation possesses exclusive regioselectivity and features mild reaction conditions and a broad substrate scope. Mechanistic studies indicated this transformation underwent a N‐alkylation‐hydroxylation‐transesterification cascade process. This research not only pushes the boundaries of the essential difunctionalization of alkenes but also exploits a new chemistry for azo compounds. [ABSTRACT FROM AUTHOR]
Copyright of Advanced Synthesis & Catalysis is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Academic Search Complete
More Details
ISSN:16154150
DOI:10.1002/adsc.202401365
Published in:Advanced Synthesis & Catalysis
Language:English