Nucleophilic Addition of Grignard Reagents to 3–Acylindoles: Stereoselective Synthesis of Highly Substituted Indoline Scaffolds-Reference-Cited by-同舟云学术

Nucleophilic Addition of Grignard Reagents to 3–Acylindoles: Stereoselective Synthesis of Highly Substituted Indoline Scaffolds

Published:2012-07-25 Issue:15 Volume:14 Page:3978-3981
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Lu¹,Shao Yushang¹,Liu Yuanhong¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, People’s Republic of China, and Department of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, People’s Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol301750b

Reference46 articles.

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

2. Catalytic Functionalization of Indoles in a New Dimension

3. Electrophilic Substitution Reactions of Indoles

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