Synthesis of Thiophene-Fused Siloles through Rhodium-Catalyzed Trans-Bis-Silylation

Akinobu Naka, Maho Inoue, Haruna Kawabe, Hisayoshi Kobayashi
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Abstract

Rhodium-catalyzed reactions of 3-ethynyl-2-pentamethyldisilanylthiophene derivatives (1a–1c) have been reported. At 110 °C, compounds 1a–1c reacted in the presence of a rhodium complex catalyst, yielding thiophene-fused siloles (2a–2c) through intramolecular trans-bis-silylation. To understand the production of 2a from 1a, the mechanism was investigated using density functional theory (DFT) calculations.
通过铑催化的反式双硅烷化合成噻吩融合的硅醇
据报道,3-乙炔基-2-五甲基二硅烷基噻吩衍生物(1a-1c)在铑催化下发生了反应。110 °C时,化合物1a-1c在铑络合物催化剂存在下发生反应,通过分子内反式二硅烷化反应生成噻吩融合硅烯(2a-2c)。为了了解 1a 生成 2a 的机理,我们使用密度泛函理论(DFT)计算进行了研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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