A carbaboranylmercuric salt catalyzed reaction; highly regioselective cycloisomerization of 1,3-dienes |
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Authors: | Yamamoto Hirofumi Sasaki Ikuo Shiomi Shinya Yamasaki Naoto Imagawa Hiroshi |
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Institution: | Faculty of Pharmaceutical Science, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan. hirofumi@ph.bunri-u.ac.jp |
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Abstract: | The combination of carbaboranylmercuric chloride (new type of bulky Lewis acid) and silver triflate efficiently catalyzes cycloisomerization of 1,3-dienes at room temperature. The catalytic system gives allyl-substituted azacycles and cycloalkanes in excellent yields with high to complete regioselectivity. |
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