Counterion Control of t ‐BuO‐Mediated Single Electron Transfer to Nitrostilbenes to Construct N ‐Hydroxyindoles or Oxindoles-Reference-Cited by-同舟云学术

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Counterion Control of t ‐BuO‐Mediated Single Electron Transfer to Nitrostilbenes to Construct N ‐Hydroxyindoles or Oxindoles

Published:2021-07-20 Issue:35 Volume:60 Page:19207-19213
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angewandte Chemie Intl Edit

Author:

Zhao Yingwei¹²,Zhu Haoran¹,Sung Siyoung³,Wink Donald J.¹,Zadrozny Joseph M.³,Driver Tom G.¹^ORCID

Affiliation:

1. Department of Chemistry University of Illinois at Chicago 845 W Taylor St. MC 111 Chicago IL 60607 USA

2. College of Chemical Engineering Huaqiao University, Xiamen 668 Jimei Boulevard Xiamen Fujian 361021 P. R. China

3. Department of Chemistry Colorado State University Fort Collins CO 80523 USA

Funder

National Science Foundation

National Institutes of Health

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202104319

Reference159 articles.

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3. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

4. An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals

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1. Intramolecular CH‐Hydrogen Bonding During the Dissociation of the Oxaphosphetane Intermediate Facilitates Z/E‐Selectivity in Wittig Olefination;ChemistryOpen;2023-12-07

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4. Denitrative Hydroxylation of Unactivated Nitroarenes**;Chemistry – A European Journal;2023-02-08

5. PPh₃-Mediated Synthesis of 3-Hydroxy-2-oxindoles from o-Alkynylnitrobenzenes;Chinese Journal of Organic Chemistry;2023

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