Dual Photoredox/Nickel-Catalyzed Conversion of Aryl Halides to Aryl Aminooxetanes: Computational Evidence for a Substrate-Dependent Switch in Mechanism-Reference-Cited by-同舟云学术

Dual Photoredox/Nickel-Catalyzed Conversion of Aryl Halides to Aryl Aminooxetanes: Computational Evidence for a Substrate-Dependent Switch in Mechanism

Published:2019-11-08 Issue:1 Volume:10 Page:405-411
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Kolahdouzan Kavoos¹,Khalaf Ryan¹,Grandner Jessica M.¹^ORCID,Chen Yongsheng²,Terrett Jack A.¹^ORCID,Huestis Malcolm P.¹^ORCID

Affiliation:

1. Discovery Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, United States

2. WuXi AppTec Co., Ltd., 288 Fute Zhong Road, Waigaoqiao Free Trade Zone, Shanghai 200131, People’s Republic of China

Funder

Genentech

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.9b03596

Reference44 articles.

1. Bioisosterism: A Rational Approach in Drug Design

2. Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design

3. Oxetanes as Versatile Elements in Drug Discovery and Synthesis

4. Evaluation of Oxetan-3-ol, Thietan-3-ol, and Derivatives Thereof as Bioisosteres of the Carboxylic Acid Functional Group

Cited by 44 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. Strain‐Release‐Driven Modular Synthesis of Oxetane‐Based Amide Bioisosteres: Concise, Robust and Scalable Approach;Angewandte Chemie;2024-09-05

2. Strain‐Release‐Driven Modular Synthesis of Oxetane‐Based Amide Bioisosteres: Concise, Robust and Scalable Approach;Angewandte Chemie International Edition;2024-09-05

3. Photoredox/Nickel Dual-Catalyzed Allylation of Aldehydes with Allylic Alcohols and Mechanistic Insights in the Presence of CO₂;ACS Catalysis;2024-08-05

4. Visible light–mediated aza Paternò–Büchi reaction of acyclic oximes and alkenes to azetidines;Science;2024-06-28

5. Modular Access to Functionalized Oxetanes as Benzoyl Bioisosteres;Journal of the American Chemical Society;2024-06-21