Switchable C2/C3 positional selectivity of thioisatins in a three-component domino reaction: combined computational and experimental studies-Reference-Cited by-同舟云学术

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Switchable C2/C3 positional selectivity of thioisatins in a three-component domino reaction: combined computational and experimental studies

Published:2022 Issue:48 Volume:20 Page:9639-9644
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liu Baolin¹,Deng Qingsong¹,Zhang Lei²^ORCID,Yu Aimin¹,Meng Xiangtai¹^ORCID

Affiliation:

1. Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Chemistry & Chemical Engineering, Tianjin University of Technology, Tianjin 300384, P. R. China

2. Tianjin Engineering Technology Center of Chemical Wastewater Source Reduction and Recycling, School of Science Tianjin Chengjian University, Tianjin 300384, P.R. China

Abstract

Switchable C2/C3 positional selectivity of thioisatins in a three-component domino reaction was studied by DFT calculations and experiments.

Funder

Tianjin Municipal Education Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01764D

Reference56 articles.

1. Enantioselective Michael/Cyclization Reaction Sequence: Scaffold-Inspired Synthesis of Spirooxindoles with Multiple Stereocenters

2. Nickel-Catalyzed Reaction of Thioisatins and Alkynes: A Facile Synthesis of Thiochromones

3. A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds

4. Efficient enantioselective synthesis of CF2H-containing dispiro[benzo[b]thiophene-oxindole-pyrrolidine]s via organocatalytic cycloaddition

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