Copper promoted synthesis of tetrazoles and further conversion into diaryl tetrazoles through C-N cross-coupling approach

313-324Efficient tandem three component method has been demonstrated for the synthesis of substituted tetrazoles under mild reaction conditions using copper catalysis. Green solvent DMSO has been utilized and the reaction has been carried out at room temperature which establishes that our method is green synthetic approach. Variety of substrates readily undergo the optimized reaction conditions to provide their respective target products in good to excellent yields. In addition we have observed regioselective compounds depending on the substituents of phenyl ring. All the reactions are rapid, facile and are accomplished at room temperature. The reactions are of general application, clean and efficient. Furthermore we have confirmed that no other by-products could be identified during our experimental reaction process. In addition, C-N cross-coupling have been developed with phenyltetrazoleamines and aryl iodide under moderate reaction conditions

Copper promoted synthesis of tetrazoles and further conversion into diaryl tetrazoles through C-N cross-coupling approach

Efficient tandem three component method has been demonstrated for the synthesis of substituted tetrazoles under mild reaction conditions using copper catalysis. Green solvent DMSO has been utilized and the reaction has been carried out at room temperature which establishes that our method is green synthetic approach. Variety of substrates readily undergo the optimized reaction conditions to provide their respective target products in good to excellent yields. In addition we have observed regioselective compounds depending on the substituents of phenyl ring. All the reactions are rapid, facile and are accomplished at room temperature. The reactions are of general application, clean and efficient. Furthermore we have confirmed that no other by-products could be identified during our experimental reaction process. In addition, C-N cross-coupling have been developed with phenyltetrazoleamines and aryl iodide under moderate reaction conditions

One-pot three-component tandem reaction: Synthesis of aryl/alkyl cyanamides libraries and their further conversion into tetrazole derivatives

<p>We have developed methodology for the synthesis of aryl/alkyl cyanamides from amines in one-pot four steps reaction using cheap, readily available and air stable copper source as catalyst under mild reaction conditions. We have also studied the application of cyanamides. In this connection, we could construct aryl tetrazolamine from cyanamides using click reaction</p