A Dearomatization/Debromination Strategy for the [4+1] Spiroannulation of Bromophenols with α,β‐Unsaturated Imines-Reference-Cited by-同舟云学术

A Dearomatization/Debromination Strategy for the [4+1] Spiroannulation of Bromophenols with α,β‐Unsaturated Imines

Published:2020-08-24 Issue:43 Volume:132 Page:19147-19151
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Ge Yicong¹,Qin Cheng¹,Bai Lu¹,Hao Jiamao¹,Liu Jingjing¹,Luan Xinjun¹^ORCID

Affiliation:

1. Key Laboratory of Synthetic Natural Functional Molecule of the Ministry of Education College of Chemistry & Materials Science Northwest University Xi'an 710127 China

Funder

National Outstanding Youth Science Fund Project of National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202008130

Reference93 articles.

1. For a pioneering example see:

2. Ueber die Einwirkung von Chlor auf Phenole

3. Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1,n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds

4. Palladium(0)-Catalyzed Intermolecular Carbocyclization of (1,n)-Diynes and Bromophenols: An Efficient Route to Tricyclic Scaffolds

5. Modular Assembly of Spirocarbocyclic Scaffolds through Pd0 -Catalyzed Intermolecular Dearomatizing [2+2+1] Annulation of Bromonaphthols with Aryl Iodides and Alkynes

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