Catalyst-Free α-Alkylation-α-Hydroxylation of Oxindole with Alcohols-Reference-Cited by-同舟云学术

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Catalyst-Free α-Alkylation-α-Hydroxylation of Oxindole with Alcohols

Published:2022-04-07 Issue:9 Volume:87 Page:5464-5471
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wu Siwei¹,Song Wei¹,Zhu Runyu¹,Hu Jingwen¹,Zhao Lin¹,Li Zheyao¹,Yu Xinhong¹^ORCID,Xia Chengcai²^ORCID,Zhao Jianhong¹

Affiliation:

1. Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education; Shanghai Key Laboratory of New Drug Design, School of Pharmacy, and State Key Laboratory of Bioengineering Reactors, East China University of Science & Technology, Shanghai 200237, People’s Republic of China

2. Institute of Pharmacology, School of Pharmaceutical Sciences, Taishan Medical University, Taian, Shandong 271016, People’s Republic of China

Funder

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02185

Reference44 articles.

1. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

2. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

3. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

4. 3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches

5. A Simple Screening Method for Antioxidants and Isolation of Several Antioxidants Produced by Marine Bacteria from Fish and Shellfish

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