Molecular hybridization-guided annulation reactions of isatins with 4-methylpent-3-en-2-one: A direct access to spirooxindole tetrahydropyranones-Reference-Cited by-同舟云学术

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Molecular hybridization-guided annulation reactions of isatins with 4-methylpent-3-en-2-one: A direct access to spirooxindole tetrahydropyranones

Published:2018-03-26 Issue:9 Volume:48 Page:1033-1039
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zhou Gen¹,Wei Qi-Di¹,Wang Guan-Lian¹,Gong Yi¹,Liu Huan-Huan¹,Liu Xiong-Li¹,Chen Lin²,Zhou Ying³

Affiliation:

1. Guizhou Engineering Center for Innovative Traditional Chinese Medicine and Ethnic Medicine, Guizhou University, Guiyang, China

2. College of Chemistry and Chemical Engineering, Guizhou Normal University, Guiyang, China

3. School of Pharmacy, Guiyang College of Traditional Chinese Medicine, Guiyang, China

Funder

the National Natural Science Foundations of China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2018.1433300

Reference16 articles.

1. Highly Enantio- and Diastereoselective Hetero-Diels-Alder Reactions Catalyzed by New Chiral Tridentate Chromium(III) Catalysts

2. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

3. Cui, H.L.; Tanaka, F. Chem Eur J. 2013, 19, 6213–6216.

4. Asymmetric synthesis of a structurally and stereochemically complex spirooxindole pyran scaffold through an organocatalytic multicomponent cascade reaction

5. Diversity-Oriented Synthesis of Oxacyclic Spirooxindole Derivatives through Ring-Closing Enyne Metathesis and Intramolecular Pauson-Khand (2+2+1) Cyclization of Oxindole Enynes

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1. Pyrans and Their Benzo Derivatives: Synthesis;Comprehensive Heterocyclic Chemistry IV;2022

2. Rapid entry to bispiro heterocycles merging five pharmacophores using phase-transfer catalysis;Tetrahedron Letters;2021-08

3. Six-Membered Ring Systems: With O and/or S Atoms;Progress in Heterocyclic Chemistry;2020

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