94645-46-2Relevant academic research and scientific papers
Cationic Cyclocodimerization. 3. Syntheses of Paracyclo(1,4)naphthalenophane and (1,4)Naphthalenophane Derivatives. Stereoselectivity Governed by the Structures of α-Naphthylmethylcarbenium Ion and 1-Vinylnaphthyl Moiety
Nishimura, Jun,Yamada, Noriyuki,Okuda, Tomohisa,Mukai, Yoshihiko,Hashiba, Hidetoshi,Oku, Akira
, p. 836 - 841 (2007/10/02)
The cationic cyclocodimerization of 1-(4-vinylnaphthyl)-3-(p-vinylphenyl)propane and 1,3-bis(4-vinylnaphthyl)propane with 2-phenylpropene, indene, 1,1-diphenylethylene, and styrene gave paracyclo(1,4)naphthalenophanes and (1,4)naphthalenophanes,
CATIONIC CYCLODIMERIZATION. 2. SYNTHESES OF (1,4)NAPHTHALENOPHANE AND PARACYCLO(1,4)NAPHTHALENOPHANE DERIVATIVES
Nishimura, Jun,Okuda, Tomohisa,Mukai, Yoshihiko,Hashiba, Hidetoshi,Oku, Akira
, p. 1495 - 1498 (2007/10/02)
1,3-Bis(4-vinylnaphthyl)propane and 1-(4-vinylnaphthyl)-3-(p-vinylphenyl)propane, were cyclocodimerized with indene to afford indenyl-substituted (1,4)naphthalenophanes and paracyclo(1,4)naphthalenophanes.
