Catalyst-Controlled Product Selectivity for Cycloaddition of Bis(indol-3-yl)-allenes to Fused Spiroindolines and Mechanistic Studies-Reference-Cited by-同舟云学术

Catalyst-Controlled Product Selectivity for Cycloaddition of Bis(indol-3-yl)-allenes to Fused Spiroindolines and Mechanistic Studies

Published:2019-10-04 Issue:20 Volume:21 Page:8250-8255
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Yan-Yan¹,Wei Yin¹^ORCID,Shi Min¹²^ORCID

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, People’s Republic of China

2. Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, Guangdong 518000, People’s Republic of China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Chinese Academy of Sciences

Shenzhen Municipality

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02992

Reference86 articles.

1. Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3

2. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

3. Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters

4. The use of spirocyclic scaffolds in drug discovery

5. Copper(I)-Catalyzed Asymmetric Desymmetrization: Synthesis of Five-Membered-Ring Compounds Containing All-Carbon Quaternary Stereocenters

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