Studies of Birch Reductive Alkylation of Substituted α-Tetralones

References

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• Compounds (2h-j) were produced in small quantities and could not be isolated in pure form. Therefore, they only could be estimated by the integration of their signals in the 1H NMR spectra of the mixture and were not characterized. Some of them were eventually isolated in pure form, as derivatives, after reduction of the carbonyl group or m-Chloroperbenzoic acid epoxidation and will be described elsewhere.
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• EIMS . (M+) 188 (88%), 173 (48 %), 160 (46%), 145 (100%), 131 (40%), 117 (30%), 103 (10%), 91 (15%), 77 (10%). The mass spectra does not belong to compound 3h/3i but to their rearrangement product as shown below.
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