Nickel-Catalyzed Asymmetric Reductive [3 + 2] Annulation of o-Haloaromatic β-Alkenyl Ketones with Alkynes via Alkene Isomerization: Enantioselective Synthesis of 1-Alkenyl 1H-Inden-1-ols-Reference-Cited by-同舟云学术

Nickel-Catalyzed Asymmetric Reductive [3 + 2] Annulation of o-Haloaromatic β-Alkenyl Ketones with Alkynes via Alkene Isomerization: Enantioselective Synthesis of 1-Alkenyl 1H-Inden-1-ols

Published:2021-07-29 Issue:16 Volume:11 Page:10115-10122
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Han Ya-Fei¹²,Li Yang²,Ouyang Xuan-Hui²,Hu Ming¹²,Tan Ze¹,Li Jin-Heng¹²³⁴^ORCID

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, China

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

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

4. School of Chemistry and Chemical Engineering, Henan Normal University, Kaifeng, Henan 475004, China

Funder

National Natural Science Foundation of China

Jiangxi Province Science and Technology Project

Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.1c02613

Reference52 articles.

1. A Novel Antimicrobial Substance in Etiolated Seedlings of Adlay

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3. Synthesis and antimycobacterial activity of prodrugs of indeno[2,1-c]quinoline derivatives

4. Polyketide biosynthesis beyond the type I, II and III polyketide synthase paradigms

5. Biomimetic Total Synthesis of Cyanosporaside Aglycons from a Single Enediyne Precursor through Site-Selectivep-Benzyne Hydrochlorination

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