Novel One-Pot Synthesis of Aziridines Carrying Sydnone Moiety and Their Biological Studies-Reference-Cited by-同舟云学术

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Novel One-Pot Synthesis of Aziridines Carrying Sydnone Moiety and Their Biological Studies

Published:2013-01 Issue:2 Volume:43 Page:301-308
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Hegde Jyothi C.,Girish K. S.,Adhikari Adithya,Kalluraya Balakrishna

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397911.2011.599102

Reference14 articles.

1. Aminolysis of Vinyl Epoxides as an Efficient Entry to N-H Vinylaziridines

2. Aziridines: epoxides’ ugly cousins?

3. Nucleophilic ring opening of aziridines

4. Remers , W. A.The Chemistry of Antitumour Antibiotics;Wiley- Interscience : New York , 1979 ; vol. 1, p.242.

5. Remers , W. A. ; Dorr , R. T.Alkaloids: Chemical and Biological Perspectives; S. W. Pelletier , (Ed.); Wiley : New York , 1988 ; vol. 6 , p. 1 .

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1. Sydnone: Synthesis, Reactivity and Biological Activities;Current Medicinal Chemistry;2023-03

2. Continuous flow system for biphasic synthesis of gem‐dichloroaziridine derivatives;Bulletin of the Korean Chemical Society;2023-01-11

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4. Aziridines and Azirines: Fused-Ring Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

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