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Synthesis of some novel tricyclic α-aminoacid esters and potential bioactive compounds via 1,2-prototropy and 1,3-APT cascade reactions

DOI: 10.1515/HC.2005.11.2.173

Source and publish data:

Heterocyclic Communications p. 173 - 180 (2005)

Update date:2022-08-11

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Authors:

Dondas, H. AliDondas, H. Ali

Dondas, Naciye YaktubayDondas, Naciye Yaktubay

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Article abstract of DOI:10.1515/HC.2005.11.2.173

Some novel cyclic α-aminoacid esters and potential bioactive compounds were prepared via thermal 1,2-prototropy- and 1,3-APT oxime nitrone-1,3-dipolar cycloaddition cascades reactions. This substrate allows the influence of the new stereocentres on the cascade to be assessed with respect to the configuration of the nitrone that is generated and the facial selectivity of the subsequent cycloaddition.

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Full text of DOI:10.1515/HC.2005.11.2.173

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Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/30/15 4:57 PM  

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