Regio- and stereoselective synthesis of new spirooxindoles via 1,3-dipolar cycloaddition reaction: Anticancer and molecular docking studies-Reference-Cited by-同舟云学术

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

Published:2018-03 Issue: Volume:180 Page:98-108
ISSN:1011-1344
Container-title:Journal of Photochemistry and Photobiology B: Biology
language:en
Short-container-title:Journal of Photochemistry and Photobiology B: Biology

Author:

Lotfy Gehad,El Ashry El Sayed H.,Said Mohamed M.,El Tamany El Sayed,Abdel Aziz Yasmine M.,Al-Dhfyan Abdullah,Al-Majid Abdullah M.,Barakat Assem

Funder

King Saud University

Publisher

Elsevier BV

Subject

Radiology Nuclear Medicine and imaging,Biophysics,Radiological and Ultrasound Technology,Radiation

Reference52 articles.

1. Stereoselective green synthesis and molecular structures of highly functionalized spirooxindole-pyrrolidine hybrids–a combined experimental and theoretical investigation;Kumar;J. Mol. Struct.,2018

2. FeCl3-catalyzed allylation reactions onto 3-hydroxy‑2‑oxindoles: formal total syntheses of bis‑cyclotryptamine alkaloids, (±)-chimonanthine, and (±)-folicanthine;Kinthada;J. Organomet. Chem.,2017

3. Construction of spiro [pyrrolidine‑3,3′‑oxindoles]−recent applications to the synthesis of oxindole alkaloids;Marti;Eur. J. Org. Chem.,2003

4. Synthesis, antimicrobial and antifungal activity of a new class of spiro pyrrolidines;Raj;Bioorg. Med. Chem.,2003

5. Catalytic asymmetric synthesis of oxindoles bearing a tetrasubstituted stereocenter at the C-3 position;Zhou;Adv. Synth. Catal.,2010

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