Issue 0, 1950
From the journal:

Journal of the Chemical Society (Resumed)

410. Alkenylation by use of lithium alkenyls. Part I. The condensation of isobutenyl-lithium with benzaldehyde and acetophenone, and the oxotropic rearrangement of the resulting carbinols. (Studies in molecular rearrangement. Part III.)

E. A. Braude  and  C. J. Timmons  

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410. Alkenylation by use of lithium alkenyls. Part I. The condensation of isobutenyl-lithium with benzaldehyde and acetophenone, and the oxotropic rearrangement of the resulting carbinols. (Studies in molecular rearrangement. Part III.)

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Article information

DOI
https://doi.org/10.1039/JR9500002000
Article type
Paper

J. Chem. Soc., 1950, 2000-2006

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410. Alkenylation by use of lithium alkenyls. Part I. The condensation of isobutenyl-lithium with benzaldehyde and acetophenone, and the oxotropic rearrangement of the resulting carbinols. (Studies in molecular rearrangement. Part III.)

E. A. Braude and C. J. Timmons, J. Chem. Soc., 1950, 2000 DOI: 10.1039/JR9500002000

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