Experimental and Theoretical DFT Study on Synthesis of Sterically Crowded 2,3,3,(4)5-Tetrasubstituted-4-nitroisoxazolidines via 1,3-Dipolar Cycloaddition Reactions Between Ketonitrones and Conjugated Nitroalkenes-Reference-Cited by-同舟云学术

Experimental and Theoretical DFT Study on Synthesis of Sterically Crowded 2,3,3,(4)5-Tetrasubstituted-4-nitroisoxazolidines via 1,3-Dipolar Cycloaddition Reactions Between Ketonitrones and Conjugated Nitroalkenes

Published:2015-08-07 Issue:5 Volume:53 Page:1424-1429
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Jasiński Radomir¹,Mróz Kamila¹,Kącka Agnieszka¹

Affiliation:

1. Institute of Organic Chemistry and Technology; Cracow University of Technology; ul. Warszawska 24 31-155 Cracow Poland

Funder

Cyfronet

Polish State Committee

Publisher

Wiley

Subject

Organic Chemistry

Reference48 articles.

1. Synthesis and biological activity of new arenediyne-linked isoxazolidines

2. Design, synthesis and biological activity evaluation of regioisomeric spiro-(indoline-isoxazolidines) in the inhibition of TNF-α-induced ICAM-1 expression on human endothelial cells

3. Novel C-2 Substituted Carbapenem Derivatives. Part II. Synthesis and Structure-activity Relationships of Isoxazolin-2-yl, Isoxazolidin-2-yl and 2-Pyrazolin-2-yl Carbapenems Generated Using 1,3-Dipolar Cycloaddition Chemistry.

4. Conjugated nitroalkenes: versatile intermediates in organic synthesis

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