Dimerization of conjugated cyclodienes

Author:

Suga Kyoichi,Watanabe Shoji,Kamma Keizo

Abstract

Dimerization of conjugated cyclodienes in the presence of lithium–naphthalene gave new dimers. 1-(2′-Cycloocten-1′-yl)-2-cyclooctene was prepared from 1,3-cyclooctadiene, 1,4-dicyclohexyliden-n-butane from 1-vinyl-1-cyclohexene, and a terpene dimer from α-phellandrene.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Lithium Naphthalenide, LN;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15

2. Lithium Naphthalene (LN);Fieser and Fieser's Reagents for Organic Synthesis;2009-12-15

3. Lithium Naphthalene (LN);Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

4. Reduction of Tetravalent Group 4 Metal Complexes Supported by an Extremely Bulky, Unsymmetrically Substituted β-Diketiminato Ligand Leading to the Regioselective CN Bond Cleavage Giving Ring-Contracted Metal-Imido Complexes;Organometallics;2006-04-01

5. Reactions of Trifluoromethylsulfenyl Chloride with 1,5-Cyclooctadiene;Phosphorus, Sulfur, and Silicon and the Related Elements;2002-05-01

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