Regio‐ and Diasteroselective C ‐Silylation of Enolate Enabled by a β‐Boronyl Group-Reference-Cited by-同舟云学术

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Regio‐ and Diasteroselective C ‐Silylation of Enolate Enabled by a β‐Boronyl Group

Published:2022-01-29 Issue: Volume: Page:
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Liu Yu¹,Zhan Miao²,Li Pengfei³

Affiliation:

1. National Drug Clinical Trial Institution GCP Office The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an Shaanxi 710061 China

2. Institute of Medical Research Northwestern Polytechnical University Xi'an Shaanxi 710072 China

3. Frontier Institute of Science and Technology Xi'an Jiaotong University, 99 Yanxiang Road, Xi'an Shaanxi 710054 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202100792

Reference58 articles.

1. Recent Advances in Transition-Metal-Catalyzed Synthetic Transformations of Organosilicon Reagents

2. Organosilicon Molecules with Medicinal Applications

3. Cationic silicon Lewis acids in catalysis

4. Quest for Novel Chemical Entities through Incorporation of Silicon in Drug Scaffolds

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1. The role of silicon in drug discovery: a review;RSC Medicinal Chemistry;2024

2. Iridium-catalyzed doubly stereoconvergent allylic alkylation of racemic α-boryl organozinc reagents;Chem Catalysis;2023-12

3. Access to Diverse Organoborons by α-Deprotonation and Functionalization of Benzylboronates;Organic Letters;2023-05-26

4. Nickel-Catalyzed [4＋2] Cyclization of Benzosilacyclobutenes and Acylsilanes;Chinese Journal of Organic Chemistry;2023

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