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An efficient fluoride-mediated O-arylation of sterically hindered halophenols with silylaryl triflates under mild reaction conditions

机译：在温和的反应条件下，有效的氟化物介导的位阻卤代酚与甲硅烷基芳基三氟甲磺酸酯的O-芳基化

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Gebara Karimi S.; Casagrande Gleison A.; Raminelli Cristiano;
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年度 2011
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1. An efficient fluoride-mediated O-arylation of sterically hindered halophenols with silylaryl triflates under mild reaction conditions [J] . Karimi S. Gebara, Gleison A. Casagrande, Cristiano Raminelli Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry . 2011 ,第22期

机译：在温和的反应条件下，有效的氟化物介导的位阻卤代酚与甲硅烷基芳基三氟甲磺酸酯的O-芳基化
2. Selenostannylation of arynes produced by silylaryl triflates under mild reaction conditions [J] . Cristiano Raminelli, Fabiano T Toledo, Jo?o V Comasseto Journal of the Brazilian Chemical Society . 2010 ,第11期

机译：甲硅烷基芳基三氟甲磺酸在温和的反应条件下产生的芳烃的亚硒酸酯化
3. Selenostannylation of Arynes Produced by Silylaryl Triflates under Mild Reaction Conditions [J] . Toledo FT, Comasseto JV, Raminelli C Journal of the Brazilian Chemical Society . 2010 ,第11期

机译：轻度反应条件下甲硅烷基芳烃三氟甲磺酸酯产生的芳烃的硒烯化
4. STUDIES ON SUZUKI COUPLING REACTIONS OF LARGE STERICALLY HINDERED SUBSTRATES [C] . Jian Sun, Zhaohui Jin, Ning Xie, International Conference on New Materials and Intelligent Manufacturing . 2018

机译：大型空次阻碍基材的铃木偶联反应研究
5. Diastereoselective Diels-Alder reactions with sterically hindered dienophiles for the total synthesis of (+)-dihydrodrimenin and related drimane natural products. [D] . Henderson, Jeff R. 2009

机译：与位阻双亲物的非对映选择性Diels-Alder反应，可合成（+）-dihydrodrimenin及其相关的drimane天然产物。
6. Palladium-Catalysed Coupling Reactions En Route to Molecular Machines: Sterically Hindered Indenyl and Ferrocenyl Anthracenes and Triptycenes and Biindenyls [O] . Michael J. McGlinchey, Kirill Nikitin 2020

机译：钯催化的偶联反应在分子机械中的应用：立体受阻的茚基和二茂铁蒽三萜烯和联茚
7. Selenostannylation of arynes produced by silylaryl triflates under mild reaction conditions [O] . Fabiano T Toledo, João V Comasseto, Cristiano Raminelli 2010

机译：Silylaryl在温和的反应条件下产生的植物甾烷基化酶

An efficient fluoride-mediated O-arylation of sterically hindered halophenols with silylaryl triflates under mild reaction conditions

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