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Regioselective Synthesis of Trichloromethyl‐Substituted Salicylates and Cyclohexenones by One‐Pot Cyclizations of 1,3‐Bis(trimethylsilyloxy)buta‐1,3‐dienes
Authors:Sebastian Reimann  Alina Bunescu  Andranik Petrosyan  Muhammad Sharif  Silke Erfle  Constantin Mamat  Tariel V Ghochikyan  Ashot S Saghyan  Anke Spannenberg  Alexander Villinger  Peter Langer
Institution:1. Institut für Chemie, Universit?t Rostock, Albert‐Einstein‐Stra?e 3a, DE‐18059 Rostock, (fax: +49‐381‐498‐6412;2. Leibniz Institut für Katalyse an der Universit?t Rostock e.V., Albert‐Einstein‐Stra?e 29a, DE‐18059 Rostock;3. Faculty of Chemistry, Yerevan State University, Alex Manoogian 1, 0025 Yerevan, Armenia;4. Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad, Pakistan;5. Scientific and Production Center ‘Armbiotechnology' of NAS RA, Gyurjyan str. 14, 0056 Yerevan, Armenia
Abstract:A variety of 6‐(trichloromethyl)salicylates (=2‐hydroxy‐6‐(trichloromethyl)benzoates) were prepared by TiCl4‐mediated cyclization of 1,3‐bis(trimethylsilyloxy)buta‐1,3‐dienes with 1,1,1‐trichloro‐4,4‐dimethoxybut‐3‐en‐2‐one. The employment of trimethylsilyl trifluoromethanesulfonate (Me3SiOTf) as Lewis acid resulted in the formation of trichloromethyl‐substituted cyclohexenones. The cyclizations proceeded with good‐to‐very‐good regioselectivities.
Keywords:Arene formation  Cyclization reactions  Salicylates  Organochlorine compounds  Silyl enol ethers
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