Journal of the American Chemical Society

The Low Temperature Halogenation of Isobutylenes

RT Arnold, WW Lee

Index: Arnold; Lee Journal of the American Chemical Society, 1953 , vol. 75, p. 5396,5399

Full Text: HTML

Citation Number: 12

Abstract

Presumably, compounds VI and VI1 cannot be formed via an attack by a chloronium ion (el+) in the first step, since this would lead to a Wagner-Meenvein rearrangement. The formation of the camphane derivatives VI11 and IX in relatively small quantities, however, is best explained in this way.

Detail

Detail

Detail

Congested C–C Bonds by Pd-Catalyzed Enantioselective Allyl–A...

[Ardolino, Michael J.; Morken, James P. Journal of the American Chemical Society, 2014 , vol. 136, # 19 p. 7092 - 7100]

Reactions of Tosylhydrazide Derivatives Having Olefinic Grou...

[Sato,T.; Homma,I. Bulletin of the Chemical Society of Japan, 1971 , vol. 44, p. 1885 - 1891]

Regiospecific addition of benzeneselenenyl halide to 1, 1-di...

[Ho, Pak-Tsun; Kolt, Ralph J. Canadian Journal of Chemistry, 1982 , vol. 60, p. 663 - 666]

Hydroxylation by cytochrome P-450 and metalloporphyrin model...

[Groves, John T.; Subramanian, Durga V. Journal of the American Chemical Society, 1984 , vol. 106, # 7 p. 2177 - 2181]

The Effect of Ring Size on Diacyl Peroxide Decompositions1, ...

[Hart; Wyman Journal of the American Chemical Society, 1959 , vol. 81, p. 4891,4896]