Efficient synthesis of novel antiproliferative steroidal spirooxindoles via the [3+2] cycloaddition reactions of azomethine ylides-Reference-Cited by-同舟云学术

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Efficient synthesis of novel antiproliferative steroidal spirooxindoles via the [3+2] cycloaddition reactions of azomethine ylides

Published:2015-10 Issue: Volume:102 Page:92-100
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Yu Bin,Sun Xiao-Nan,Shi Xiao-Jing,Qi Ping-Ping,Zheng Yi-Chao,Yu De-Quan,Liu Hong-Min

Funder

Natural Science Foundation of China

Development Foundation of Priority, Ministry of Education

2013 Yong Teacher Foundation

Key Scientific Research Project for Higher Education

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference62 articles.

1. Electronic structure and biological activity of steroids

2. A Review on Synthetic and Natural Steroid Dimers: 1997-2006

3. An overview of synthetic approaches for heterocyclic steroids

4. Synthesis and biological testing of steroid derivatives as inhibitors

5. Novel modified steroid derivatives of androstanolone as chemotherapeutic anti-cancer agents

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1. Optimization of the synthesis of 21-benzylidene-substituted steroids and pitfalls of the Claisen-Schmidt condensation;Russian Chemical Bulletin;2023-12

2. Design and development of novel spiro-oxindoles as potent antiproliferative agents using quantitative structure activity based Monte Carlo method, docking molecular, molecular dynamics, free energy calculations, and pharmacokinetics /toxicity studies;Journal of Molecular Structure;2023-07

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4. Synthesis, biological activities, and future perspectives of steroidal monocyclic pyridines;RSC Medicinal Chemistry;2023

5. Solvent‐free Darzens condensation of 3‐ chlorooxindoles with aryl aldehydes for diastereoselective construction of spiro‐epoxyoxindoles by grinding;Journal of Heterocyclic Chemistry;2022-12-21

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