Expanding the scope of the Cu assisted Suzuki–Miyaura reaction
摘要:
Recent advances in the development of the copper facilitated Suzuki-Miyaura reaction are described. Improvements include expansion of substrate scope to include aryl chlorides and polyhalo aryl boronates. It was found that use of S-Phos and X-Phos could accomplish the coupling of 2-pyridyl boronates to aryl chlorides and bromides in shorter reaction times and in higher yield than previously described with DPPF. (C) 2011 Elsevier Ltd. All rights reserved.
[EN] TRICYCLIC COMPOUNDS AS ANTICANCER AGENTS<br/>[FR] COMPOSÉS TRICYCLIQUES COMME AGENTS ANTI-CANCERS
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2015100282A1
公开(公告)日:2015-07-02
The present invention is directed to tricyclic compounds (I), pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.
Design and synthesis of tricyclic benzo[1, 3]oxazinyloxazolidinones as blood coagulation factor Xa inhibitors
作者:Haijia Lu、Yongqi Wu、Hongyi Zhao、Dongfeng Zhang
DOI:10.1080/00397911.2022.2079991
日期:2022.4.18
NOVEL TRICYCLIC COMPOUNDS AS ANTICANCER AGENTS
申请人:BRISTOL-MYERS SQUIBB COMPANY
公开号:US20160176864A1
公开(公告)日:2016-06-23
The present invention is directed to tricyclic compounds, pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.
本发明涉及三环化合物,包括本发明化合物的药用可接受组合物以及在治疗各种疾病中使用所述组合物的方法。
Expanding the scope of the Cu assisted Suzuki–Miyaura reaction
作者:Brendan M. Crowley、Craig M. Potteiger、James Z. Deng、Christopher K. Prier、Daniel V. Paone、Christopher S. Burgey
DOI:10.1016/j.tetlet.2011.07.088
日期:2011.9
Recent advances in the development of the copper facilitated Suzuki-Miyaura reaction are described. Improvements include expansion of substrate scope to include aryl chlorides and polyhalo aryl boronates. It was found that use of S-Phos and X-Phos could accomplish the coupling of 2-pyridyl boronates to aryl chlorides and bromides in shorter reaction times and in higher yield than previously described with DPPF. (C) 2011 Elsevier Ltd. All rights reserved.