Copper‐Catalyzed Addition of Grignard Reagents to in situ Generated Indole‐Derived Vinylogous Imines-Reference-Cited by-同舟云学术

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Copper‐Catalyzed Addition of Grignard Reagents to in situ Generated Indole‐Derived Vinylogous Imines

Published:2020-11-09 Issue:69 Volume:26 Page:16277-16280
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Ge Luo¹,Zurro Mercedes¹,Harutyunyan Syuzanna R.¹^ORCID

Affiliation:

1. Stratingh Institute for Chemistry University of Groningen Nijenborgh 4 9747 AG Groningen The Netherlands

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Fundación Ramón Areces

China Scholarship Council

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004232

Reference55 articles.

1.

2. Recent progress in the chemistry of the monoterpenoid indole alkaloids

3. Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases

4. Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinonesviaa Redox Economic Approach

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2. Merging Photoredox with Nickel Catalysis for Decarboxylative Arylation of Indole‐3‐Acetic Acids with Aryl Halides;ChemPhotoChem;2024-03-06

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4. Catalytic Access to 4-(sec-Alkyl)Anilines via 1,6-Conjugate Addition of Grignard Reagents to in Situ Generated aza-p-Quinone Methides;Organic Letters;2022-09-02

5. ASYMMETRIC NUCLEOPHILIC ADDITION TO KETONES AND KETIMINES AND CONJUGATE ADDITION REACTIONS;Catalytic Asymmetric Synthesis;2022-06-03

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