Nucleophilic Dearomatization of Chloromethyl Naphthalene Derivatives via η3-Benzylpalladium Intermediates: A New Strategy for Catalytic Dearomatization-Reference-Cited by-同舟云学术

Nucleophilic Dearomatization of Chloromethyl Naphthalene Derivatives via η3-Benzylpalladium Intermediates: A New Strategy for Catalytic Dearomatization

Published:2011-09-13 Issue:19 Volume:13 Page:5402-5405
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Peng Bo¹,Zhang Sheng¹,Yu Xiaoqiang¹,Feng Xiujuan¹,Bao Ming¹

Affiliation:

1. State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2023278

Reference34 articles.

1. Nucleophilic Dearomatizing (DNAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis

2. Oxidative Dearomatization of Phenols: Why, How and What For?

3. Hypervalent iodine-mediated phenol dearomatization in natural product synthesis

4. Dearomatization Strategies in the Synthesis of Complex Natural Products

5. Palladium-Catalyzed Asymmetric Dearomatization of Naphthalene Derivatives

Cited by 60 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Palladium‐Catalyzed Synthesis of Bicyclic Derivatives from the Cyclization/1,4‐Difunctionalization of Bromoarenes with Diazo Compounds;Asian Journal of Organic Chemistry;2023-12-14

2. Pd-Catalyzed Intramolecular Dearomative [4 + 2] Cycloaddition of Naphthalenes with Arylalkynes;Organic Letters;2023-11-07

3. Palladium-Catalyzed Para-C–H Bond Amination of 2-Aryl Chloromethylbenzenes;The Journal of Organic Chemistry;2022-07-28

4. Confronting the Challenging Asymmetric Carbonyl 1,2-Addition Using Vinyl Heteroarene Pronucleophiles: Ligand-Controlled Regiodivergent Processes through a Dearomatized Allyl–Cu Species;Journal of the American Chemical Society;2022-03-26

5. Dearomative spirocyclization via visible-light-induced reductive hydroarylation of non-activated arenes;Chinese Chemical Letters;2022-01