Organocatalytic Regio- and Enantioselective 1,8-Additions of Nitrogen and Sulfur Nucleophiles to 6-Methylene-6H-indoles-Reference-Cited by-同舟云学术

Organocatalytic Regio- and Enantioselective 1,8-Additions of Nitrogen and Sulfur Nucleophiles to 6-Methylene-6H-indoles

Published:2020-09-29 Issue:20 Volume:22 Page:7859-7863
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Song Qianqian¹,Zhang Pei¹,Liang Shuai¹,Chen Xuling²,Li Pengfei²³^ORCID,Li Wenjun¹^ORCID

Affiliation:

1. Department of Medicinal Chemistry, School of Pharmacy, Qingdao University, Qingdao 266021, China

2. Shenzhen Grubbs Institute and Department of Chemistry, College of Science, Southern University of Science and Technology (SUSTech), Shenzhen 518055, China

3. Guangdong Provincial Key Laboratory of Catalysis, SUSTech, Shenzhen 518055, China

Funder

Shandong Province

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c02769

Reference67 articles.

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2. New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems

3. Aminocatalytic remote functionalization strategies

4. Conjugate addition reactions of carbon nucleophiles to electron-deficient dienes

5. Organocatalytic Asymmetric 1,6-Addition Reactions

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