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  • Acids direct 2-styrylcyclobutanone into two distinctly different reaction pathways.

Acids direct 2-styrylcyclobutanone into two distinctly different reaction pathways.

Organic letters (2005-05-07)
Masahiro Murakami, Sho Kadowaki, Atsushi Fujimoto, Mitsuru Ishibashi, Takanori Matsuda
ABSTRACT

Two structurally distinct carbocycles were selectively obtained by the reactions of 2-(o-styryl)cyclobutanones promoted by ytterbium salts. Treatment of the cyclobutanones with YbCl(3) in 1,4-dioxane at 100 degrees C afforded 2-(2-chloroethyl)naphthalenes. On the other hand, the reaction with Yb(OTf)(3) in chlorobenzene at 130 degrees C gave 9,10-dihydrobenzocycloocten-7(8H)-ones.

MATERIALS
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Brand
Product Description

Sigma-Aldrich
Vinylboronic anhydride pyridine complex, 95%