- Development and Mechanistic Studies of Iron-Catalyzed Construction of Csp2-B Bonds via C-O Bond Activation
-
Herein we describe an iron-catalyzed borylation of alkenyl and aryl carbamates through the activation of a C-O bond. This protocol exhibits high efficiency, a broad substrate scope, and the late-stage borylation of biorelevant compounds, thus providing potential applications in medicinal chemistry. Moreover, this method enables orthogonal transformations of phenol derivatives and also offers good opportunities for the synthesis of multisubstituted arenes. Preliminary mechanistic studies suggest that a FeII/FeIII catalytic cycle via a radical pathway might be involved in the reaction.
- Geng, Shasha,Zhang, Juan,Chen, Shuo,Liu, Zhengli,Zeng, Xiaoqin,He, Yun,Feng, Zhang
-
p. 5582 - 5588
(2020/07/08)
-
- COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME
-
The present invention provides a compound represented by chemical formula and an organic light emitting device comprising the same. The organic light emitting device comprising the compound has excellent electrochemical and thermal stability, thereby having excellent lifespan characteristics.COPYRIGHT KIPO 2020
- -
-
-
- LiHMDS-Promoted Palladium or Iron-Catalyzed ipso-Defluoroborylation of Aryl Fluorides
-
A novel and efficient method for the synthesis of arylboronic acid pinacol esters via a palladium- or iron-catalyzed cross-coupling reaction of aryl fluorides with bis(pinacolato)diboron (B2pin2) in the presence of LiHMDS was developed. The Pd-catalyzed defluoroborylation of fluoroarenes is compatible with a variety of functional groups such as primary and secondary amine, ketone, trifluoromethyl, alkoxy, and boryl. Remarkably, no external ligand is required for enhanced conversion efficiency.
- Zhao, Xianghu,Wu, Mingsheng,Liu, Yisen,Cao, Song
-
supporting information
p. 5564 - 5568
(2018/09/12)
-
- COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF
-
The present invention relates to: a compound which can obtain high light emitting efficiency and low driving voltage of a device and expand lifespan of the device; an organic electric device using the same; and an electronic apparatus thereof. The present invention provides a compound represented by chemical formula 1, and provides an organic electric device using the compound represented by the chemical formula and an electronic apparatus thereof.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transport layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transport layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2016
- -
-
Paragraph 0343-0344
(2016/10/07)
-
- COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF
-
The present invention relates to: a compound which can obtain high light emitting efficiency and low driving voltage of a device and expand lifespan of the device; an organic electric device using the same; and an electronic apparatus thereof. The present invention provides a compound represented by chemical formula 1, and provides an organic electric device using the compound represented by the chemical formula and an electronic apparatus thereof.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transport layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transport layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2016
- -
-
Paragraph 0165; 0174
(2016/10/07)
-
- MATERIAL FOR ORGANIC PHOTOELECTRIC DEVICE INCLUDING ELECTRON TRANSPORTING UNIT AND HOLE TRANSPORTING UNIT, AND ORGANIC PHOTOELECTRIC DEVICE INCLUDING THE SAME
-
A material for an organic photoelectric device, the material including a compound including a pyridine ( ) moiety, the compound being a bipolar organic compound including both a hole transporting unit and an electron transporting unit, the compound being represented by the following Formula 1:
- -
-
Page/Page column 23-24
(2012/11/13)
-