Diversity‐Oriented Synthesis of α‐Functionalized Acylborons and Borylated Heteroarenes by Nucleophilic Ring Opening of α‐Chloroepoxyboronates-Reference-Cited by-同舟云学术

Diversity‐Oriented Synthesis of α‐Functionalized Acylborons and Borylated Heteroarenes by Nucleophilic Ring Opening of α‐Chloroepoxyboronates

Published:2019-09-23 Issue:39 Volume:58 Page:13784-13788
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Tan Dong‐Hang¹,Cai Yuan‐Hong¹,Zeng Yao‐Fu¹,Lv Wen‐Xin¹,Yang Ling¹,Li Qingjiang¹,Wang Honggen¹²^ORCID

Affiliation:

1. Guangdong Key Laboratory of Chiral Molecule and Drug DiscoverySchool of Pharmaceutical SciencesSun Yat-sen University Guangzhou 510006 China

2. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal ResourcesSchool of Chemistry and Pharmaceutical Sciences ofGuangxi Normal University Guilin 541004 China

Funder

the Key Project of Chinese National Programs for Fundamental Research and Development

the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201907349

Reference112 articles.

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3. Synthesis of Chemically and Configurationally Stable Monofluoro Acylboronates: Effect of Ligand Structure on their Formation, Properties, and Reactivities

4. Amphoteric α-Boryl Aldehyde Linchpins in the Synthesis of Heterocycles

5. Synthesis and reactivities of monofluoro acylboronates in chemoselective amide bond forming ligation with hydroxylamines

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