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Behavior of [2.n]metacyclophanes-fused cyclobutane ring in bromination

✍ Scribed by Yukihiro Okada; Masanori Yokozawa; Masatoshi Kaneko; Jun Nishimura


Book ID
104251566
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
80 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


Dimethoxy[2.2]metacyclophane mainly gave a tetrahydropyrene structure and the other [2.n]metacyclophane derivatives (n=3-5) gave aromatic bromides like pseudo-ipso and/or pseudo-ortho dibromides in the reaction with bromine. They also gave benzyl bromides by cyclobutane ring-opening.