Journal of the Chemical Society. Chemical communications p. 561 - 562 (1981)
Update date:2022-08-02
Topics:
Abramovitch, Rudolph A.
Abramovitch, Dorota A.
Tomasik, Piotr
The isolation of radical coupling products and the observation of appropriate C.I.N.D.P. signals suggest that most of the title reactions proceed by homolysis of the anhydro-bases (4) or (9) followed by radical recombinations; a diazo-oxy-Cope rearrangement may still account for the formation of α-acylamination products.
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