Transition Metal-catalyzed Fixation of Carbon Dioxide via Carbon-carbon Bond Formation

被引：8

作者：

Fujihara, Tetsuaki ^{[1
]}

Tsuji, Yasushi ^{[1
]}

机构：

[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

来源：

JOURNAL OF THE JAPAN PETROLEUM INSTITUTE | 2016年 / 59卷 / 03期

关键词：

Carbon dioxide; Homogeneous catalysis; Nickel catalyst; Copper catalyst; Carbon-carbon bond formation; HOMOGENEOUS HYDROGENATION; REDUCTIVE CARBOXYLATION; ALKENYLBORONIC ESTERS; UNACTIVATED PRIMARY; 2+2+2 CYCLOADDITION; CO2; ALKYNES; COPPER; COMPLEXES; HYDROCARBOXYLATION;

D O I：

10.1627/jpi.59.84

中图分类号：

TE [石油、天然气工业]; TK [能源与动力工程];

学科分类号：

0807 ; 0820 ;

摘要：

Carbon dioxide (CO2) is a readily available carbon source, but the thermodynamic characteristics of CO2 limit its widespread use in chemical reactions. This review summarizes the transformation of CO2 via carbon-carbon bond-forming reactions. Ni complexes catalyzed the carboxylation of less reactive aryl chlorides and double carboxylation of internal alkynes in the presence of suitable reducing agents such as Mn or Zn powders under 1 atm of CO2. Using Cu complexes as catalysts under CO2 atmosphere, hydrocarboxylation and silacarboxylation of alkynes proceeded efficiently using hydrosilanes and silylboranes, respectively, as the reagents.

引用

页码：84 / 92

页数：9

共 65 条

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