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Rhenium‐ and Manganese‐Catalyzed Insertion of Alkynes into a Carbon–Carbon Single Bond of Cyclic and Acyclic 1,3‐Dicarbonyl Compounds
Authors:Yoichiro Kuninobu Dr.  Atsushi Kawata  Mitsumi Nishi  Salprima Yudha S.  Jingjin Chen  Kazuhiko Takai Prof. Dr.
Affiliation:1. Division of Chemistry and Biochemistry, Graduate School of Natural Science and Technology, Okayama University, Tsushima, Kita‐ku, Okayama 700‐8530 (Japan), Fax: (+81)?86‐251‐8094;2. Current address: Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)
Abstract:Treatment of alkynes with cyclic and acyclic 1,3‐dicarbonyl compounds in the presence of a catalytic amount of a rhenium or manganese complex gives ring‐expanded and carbon‐chain extension products, respectively. In these reactions, alkynes insert into a non‐strained carbon–carbon single bond of 1,3‐dicarbonyl compounds. The ring‐expansion reaction is also promoted by the addition of 4‐Å molecular sieves instead of a catalytic amount of an isocyanide.
Keywords:alkynes  C?C activation  insertion  manganese  rhenium
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