ChemInform Abstract: NUCLEOPHILIC DISPLACEMENT CATALYZED BY TRANSITION METALS. PART IV. SYNTHESIS OF ARYL IODIDES FROM ARYL HALIDES AND POTASSIUM IODIDE BY MEANS OF A NICKEL CATALYST

1978 ◽  
Vol 9 (40) ◽  
Author(s):  
K. TAKAGI ◽  
N. HAYAMA ◽  
T. OKAMOTO
Keyword(s):  
Transition Metals ◽  
Nickel Catalyst ◽  
Potassium Iodide ◽  
Aryl Halides ◽  
Aryl Iodides ◽  
Nucleophilic Displacement

scholarly journals SYNTHESIS OF ARYL IODIDES FROM ARYL HALIDES AND POTASSIUM IODIDE BY MEANS OF NICKEL CATALYST

1978 ◽  
Vol 7 (2) ◽  
pp. 191-192 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Tadashi Okamoto
Keyword(s):  
Nickel Catalyst ◽  
Potassium Iodide ◽  
Aryl Halides ◽  
Aryl Iodides

ChemInform Abstract: NUCLEOPHILIC DISPLACEMENT CATALYZED BY TRANSITION METALS. I. CYANATION OF ARYL HALIDES CATALYZED BY PALLADIUM(II)

1976 ◽  
Vol 7 (7) ◽  
pp. no-no
Author(s):  
KENTARO TAKAGI ◽  
TADASHI OKAMOTO ◽  
YASUMASA SAKAKIBARA ◽  
ATSUYOSHI OHNO ◽  
SHINZABURO OKA ◽  
...  
Keyword(s):  
Transition Metals ◽  
Aryl Halides ◽  
Nucleophilic Displacement

A Nickel/Organoboron Catalyzed Metallaphotoredox Platform for C(sp2)–P and C(sp2)–S Bond Construction

2022 ◽  
Author(s):  
Yuan Zhu ◽  
Weisai Zu ◽  
Qing Tian ◽  
Zifeng Cao ◽  
Yu Wei ◽  
...  
Keyword(s):  
Nickel Catalyst ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Herein, an organoboron photocatalyst, aminoquinolate diarylboron (AQDAB), is utilized collaboratively with nickel catalyst in metallaphotoredox catalyzed C(sp2)–P and C(sp2)–S cross-coupling reactions. This strategy effectively couples aryl halides with diarylphosphine oxides...

scholarly journals Nickel-catalyzed C–N bond activation: activated primary amines as alkylating reagents in reductive cross-coupling

2019 ◽  
Vol 10 (16) ◽  
pp. 4430-4435 ◽  
Author(s):  
Huifeng Yue ◽  
Chen Zhu ◽  
Li Shen ◽  
Qiuyang Geng ◽  
Katharina J. Hock ◽  
...  
Keyword(s):  
Nickel Catalyst ◽  
Bond Activation ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Primary Amines ◽  
Pyridinium Salts ◽  
Reaction Conditions ◽  
Alkyl Amines ◽  
Alkylating Reagents

The reductive cross coupling of pyridinium salts derived from readily available primary alkyl amines with aryl halides has been achieved under mild reaction conditions using a nickel catalyst.

scholarly journals SYNTHESIS OF BIARYLS FROM ARYL IODIDES AND ZINC POWDER BY MEANS OF NICKEL CATALYST

1979 ◽  
Vol 8 (8) ◽  
pp. 917-918 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Saburo Inokawa
Keyword(s):  
Nickel Catalyst ◽  
Zinc Powder ◽  
Aryl Iodides

Visible-Light-Driven Reductive Carboarylation of Styrenes with CO2 and Aryl Halides

2019 ◽  
Author(s):  
Hao Wang ◽  
yuzhen gao ◽  
Chunlin Zhou ◽  
Gang Li
Keyword(s):  
Visible Light ◽  
Alkyl Halides ◽  
Aryl Halides ◽  
Addition Reactions ◽  
Aryl Chlorides ◽  
Aryl Iodides ◽  
Visible Light Driven ◽  
User Friendly

The first example of visible-light-driven reductive carboarylation of styrenes with CO<sub>2</sub> and aryl halides in a regioselective manner has been achieved. A broad range of aryl iodides and bromides were compatible with this reaction. <a>Moreover, pyridyl halides, alkyl halides and even aryl chlorides were also viable with this method.</a> These findings may stimulate the exploration of novel visible-light-driven Meerwein arylation-addition reactions with user-friendly aryl halides as the radical sources and the photocatalytic utilization of CO<sub>2.</sub>

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