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Acid Promoted New Carbon-Hydrogen Bond Cleavage Mechanism in 2-Allylphenoxoruthenium(II) Complex

机译:酸促进2-烯丙基氧氧氧氧氧鎓(II)复合物中的新型碳 - 氢粘合裂解机制

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C-H Bond cleavage reactions by ruthenium complexes have been extensively studied due to their potential utility in organic synthesis. One of the important factors for C-H bond cleavage reaction is prior coordination or binding through an anchoring group to bring the unactivated C-H bond in proximity to the ruthenium center. Recently, we found that Bronsted acids effectively promoted intramolecular C-H bond cleavage reaction of RuCp[OC6H4(CH2CH=CH2-2)-K~1O](PPh3)2 (1), leading to RuCp[CH2CHCH(C6H4OH-2)-η~3C,C',C"](PPh3) (3) under ambient conditions. Herein we report a new type acid-promoted C-H bond cleavage reaction, that involvs a 6 membered transition-state concerning two acid molecules.
机译:由于它们在有机合成中的潜在效用,钌配合物的C-H键裂解反应已经过度研究。 C-H键裂解反应的重要因素之一是通过锚定基团的结合或结合,以使未激活的C-H键与钌中心的邻近。最近,我们发现伪造酸有效地促进了RUCP [OC6H4(CH2CH = CH2-2)-K〜1O](PPH3)2(1)的分子内CH键裂解反应,所述RUCP [CH 2 CHCH(C6H4OH-2)-η在环境条件下〜3C,C',C“](PPH3)(3)。在本文中,我们报告了一种新型酸促进的CH键切割反应,其涉及关于两个酸分子的6元转变状态。

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