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Single electron transfer reductive cleavage of the aryl-nitrogen bond in phenyl-substituted dimethylanilines

✍ Scribed by U. Azzena; F. Dessanti; G. Melloni; L. Pisano


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
216 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


By treatment with Li metal in THF at room temperature the three isomeric N,N-dimethylaminobiphenyls and NJ-dimethyl-2,6-diphenylanilineunderwent 100% regioselective reductive cleavage of the aryl-N bond, affording biphenyl and me&-terphenyl, respectively, in various yields.


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