Synthesis of chiral spiro-cyclopentene/cyclopentadiene-oxindoles through an asymmetric [3 + 2] cycloaddition of isatin-derived MBH carbonates and β,γ-unsaturated α-keto esters-Reference-Cited by-同舟云学术

Synthesis of chiral spiro-cyclopentene/cyclopentadiene-oxindoles through an asymmetric [3 + 2] cycloaddition of isatin-derived MBH carbonates and β,γ-unsaturated α-keto esters

Published:2019-05 Issue:21 Volume:75 Page:2971-2979
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chen Yu,Cui Bao-Dong,Bai Mei,Han Wen-Yong,Wan Nan-Wei,Chen Yong-Zheng

Funder

National Nature Science Foundation of China

National First-Rate Construction Discipline of Guizhou Province (Pharmacy)

Program for Outstanding Youth of Zunyi Medical University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. For reviews, see:

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

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

4. Organocatalytic asymmetric synthesis of 3-amino-2-oxindole derivatives bearing a tetra-substituted stereocenter

5. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

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