64884-78-2Relevant academic research and scientific papers
Synthetic Routes for Heteroatom-Containing Alkylated/Arylated Polycyclic Aromatic Hydrocarbons
Shi, Qinqin,Shi, Xiaosong,Feng, Changfu,Wu, Yishi,Zheng, Nan,Liu, Jie,Wu, Xiaoxi,Chen, Hao,Peng, Aidong,Li, Jianfeng,Jiang, Lang,Fu, Hongbing,Xie, Zengqi,Marder, Seth R.,Blakey, Simon B.,Huang, Hui
, p. 2924 - 2928 (2021)
Synthetic routes for heteroatom-containing polycyclic aromatic hydrocarbons (H-PAHs) with alkyl and aryl substitution are demonstrated. Three H-PAHs, including heteroatom-containing rubicenes (H-rubicenes), angular-benzothiophenes (ABTs), and indenothioph
Palladium-Catalyzed Cross-Coupling of gem-Bis(boronates) with Aryl Halides: An Alternative to Access Quaternary α-Aryl Aldehydes
Zheng, Purui,Zhai, Yujie,Zhao, Xiaoming,Xu, Tao
supporting information, p. 393 - 396 (2019/01/23)
The compounds with a quaternary α-aryl aldehyde skeleton are important units in organic chemistry. Previously, the aryl group and carbonyl group are introduced in a stepwise manner. Herein, a novel route is developed to construct the quaternary α-aryl aldehydes with gem-bis(boronates) as precursors, in which the two groups are installed simultaneously. The gem-bis(boronates) are readily available from ketones; as a result, this methodology provides a more general strategy to produce the quaternary α-aryl aldehydes with broad scopes and synthetic convenience.
Difunctionalization of ketones: Via gem -bis(boronates) to synthesize quaternary carbon with high selectivity
Zheng, Purui,Zhai, Yujie,Zhao, Xiaoming,Xu, Tao
supporting information, p. 13375 - 13378 (2018/12/13)
All-carbon quaternary centres are significant and prevalent structural frameworks but their preparation routes are rare and challenging, especially methods with common substrates. Herein, we report a convenient process to construct all-carbon quaternary c
