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Synthesis and evolution of new isoxazolo-1,4-quinones of biologic interest

DOI: 10.1515/HC.2006.12.6.457

Source and publish data:

Heterocyclic Communications p. 457 - 462 (2006)

Update date:2022-07-29

Topics:

Authors:

Hamadi, Naoufel BenHamadi, Naoufel Ben

Msaddek, MoncefMsaddek, Moncef

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Article abstract of DOI:10.1515/HC.2006.12.6.457

In the exploration of synthesis and chemistry of isoxazoles, we found that the reaction of aromatic nitrile oxides with the Quinone derivatives produced isoxazolo-1,4-quinones is of considerable biological interest. The reductive cleavage of the N-O bond

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Full text of DOI:10.1515/HC.2006.12.6.457

Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  
Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  
Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  
Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  
Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  
Brought to you by | Brown University Rockefeller Library  
Authenticated | 128.148.252.35  
Download Date | 9/3/13 4:55 PM  

Products guided by the article

Product name:Naphth[2,3-d]isoxazole-4,9-dione, 3-(4-methylphenyl)-

Cas No:37976-15-1

37976-15-1

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