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Cationic cyclocodimerization. 3. Syntheses of [3.3]paracyclo(1,4)naphthalenophane and [3.3](1,4)naphthalenophane derivatives. Stereoselectivity governed by the structures of .alpha.-naphthylmethylcarbenium ion and 1-vinylnaphthyl moiety

✍ Scribed by Nishimura, Jun; Yamada, Noriyuki; Okuda, Tomohisa; Mukai, Yoshihiko; Hashiba, Hidetoshi; Oku, Akira


Book ID
127258568
Publisher
American Chemical Society
Year
1985
Tongue
English
Weight
709 KB
Volume
50
Category
Article
ISSN
0022-3263

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Cationic cyclocodimerization. 2. Synthes
✍ Jun Nishimura; Tomohisa Okuda; Yoshihiko Mukai; Hidetoshi Hashiba; Akira Oku πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 224 KB

1,3-Bis(4-vinylnaphthyl)propane and 1-(4-vinylnaphthylj-3-(p-vinylphenyllpropane, were cyclocodimerized with indene to afford indenyl-substituted [3\_3](1,4)naphthalenophanes and [3.3]paracyclo(l,4)naphthalenophanes. Syntheses of [3.3](l,4)naphthalenophane2