Syntheses of Isoprenoids from Isoprene. III. The Dimerizations of Dimethylcyclopropanes

doi:10.1246/BCSJ.45.3147

Paper

Syntheses of Isoprenoids from Isoprene. III. The Dimerizations of Dimethylcyclopropanes

Published Oct 1, 1972 · J. Tanaka, T. Katagiri, K. Takabe

Bulletin of the Chemical Society of Japan

Q2 SJR score

3

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0

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Abstract

1,1-Dimethylcyclopropane(I) was found to dimerize selectively by the action of boron trifluoride etherate. In the products, compound (III), which had been presumed, and the reaction intermediates (VII and VIII) were identified. The reaction mechanism was discussed. 1,2-Dimethylcyclopropane(VI) gave the same products.

Study Snapshot

Boron trifluoride etherate selectively dimerizes 1,1-dimethylcyclopropane(I) to produce isoprenoids (III) and reaction intermediates (VII and VIII).

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Syntheses of Isoprenoids from Isoprene. III. The Dimerizations of Dimethylcyclopropanes

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