Palladium‐Catalyzed Reductive [5+1] Cycloaddition of 3‐Acetoxy‐1,4‐enynes with CO: Access to Phenols Enabled by Hydrosilanes-Reference-Cited by-同舟云学术

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Palladium‐Catalyzed Reductive [5+1] Cycloaddition of 3‐Acetoxy‐1,4‐enynes with CO: Access to Phenols Enabled by Hydrosilanes

Published:2018-10 Issue:40 Volume:57 Page:13308-13312
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Wu Li‐Jun¹²,Song Ren‐Jie¹²,Luo Shenglian¹²,Li Jin‐Heng¹²³^ORCID

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and ChemometricsHunan University Changsha 410082 China

2. Key Laboratory of Jiangxi Province for Persistent, Pollutants Control and Resources RecycleNanchang Hangkong University Nanchang 330063 China

3. State Key Laboratory of Applied Organic ChemistryLanzhou University Lanzhou 730000 China

Funder

the Natural Science Foundation of China

the Jiangxi Province Science and Technology Project

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201808388

Reference88 articles.

1. For selected reviews see:

2. Transition metal-mediated cycloaddition reactions of alkynes in organic synthesis

3. Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way

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4. [2+2+1+1] Cycloaddition for de novo Synthesis of Densely Functionalized Phenols;Angewandte Chemie International Edition;2023-07-24

5. [2+2+1+1] Cycloaddition for de novo Synthesis of Densely Functionalized Phenols;Angewandte Chemie;2023-07-24

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