Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 73, Issue 20, Pages 8124-8127Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo801751a
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- EaStChem
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Acyl oximes derived from a variety of indolylalkanones underwent a ring closure sequence during FVP to afford 9H-pyrido[2,3-b]indoles. Unlike UV light promoted reactions of oxime esters, the mechanism is almost certainly not mediated by iminyl radicals but probably involves tautomerism, elimination of acetic acid, and a final electrocyclic ring closure.
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