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Silaphenylmercuric Triflate Catalyzed Reactions: Synthesis of a Solid‐Supported Mercuric Salt Catalyst
Authors:Hirofumi Yamamoto  Ikuo Sasaki  Yuki Hirai  Kosuke Namba  Hiroshi Imagawa  Mugio Nishizawa Prof
Institution:Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro‐cho, Tokushima 770‐8514 (Japan), Fax: (+81)?88‐655‐3051 http://p.bunri‐u.ac.jp/~nishizaw/e‐home/e‐index.html
Abstract:Let it flow, let it flow : A procedure to generate the first solid‐supported mercuric salt, silaphenylmercuric triflate, is described. Silaphenylmercuric triflate showed remarkable catalytic activity for an indole synthesis, furanoyne cyclization, arylyne cyclization, and tandem carbocyclizations. An efficient flow reaction system for indole synthesis and arylyne cyclization is also described (see figure).
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Keywords:alkynes  cyclization  flow reactor  heterocycles  mercury
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