Diastereoselective 1,3-dipolar cycloaddition of cyclopropenes to acenaphthenequinone azomethine ylides-Reference-Cited by-同舟云学术

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Diastereoselective 1,3-dipolar cycloaddition of cyclopropenes to acenaphthenequinone azomethine ylides

Published:2024-01 Issue: Volume:151 Page:133792
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Stepakov Alexander V.,Pronina Yulia A.,Filatov Alexander S.,Selivanov Stanislav I.,Kornev Anton A.,Kryukova Mariya A.,Ponyaev Alexander I.,Boitsov Vitali M.

Funder

Ministry of Education and Science of the Russian Federation

Saint Petersburg State University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference53 articles.

1. New and unusual scaffolds in medicinal chemistry

2. The use of spirocyclic scaffolds in drug discovery

3. Design and Synthesis of Spirocycles

4. Design, synthesis, molecular docking and biological activity evaluation of some novel indole derivatives as potent anticancer active agents and apoptosis inducers

5. Regio- and stereoselective synthesis of new spirooxindoles via 1,3-dipolar cycloaddition reaction: Anticancer and molecular docking studies

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Organocatalytic Diastereoselective Synthesis of Spiro[3-azabicyclo[3.1.0]hexanes] via 1,3-Dipolar Cycloaddition of Azomethine Ylides with Cyclopropenes;Russian Journal of General Chemistry;2024-04

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