ChemInform Abstract: Metal-Free Decarboxylative Three-Component Coupling Reaction for the Synthesis of Propargylamines.

ChemInform ◽  
2013 ◽  
Vol 44 (48) ◽  
pp. no-no
Author(s):  
Kyungho Park ◽  
Yumi Heo ◽  
Sunwoo Lee
Keyword(s):  
Coupling Reaction ◽  
Metal Free ◽  
Three Component Coupling

Metal-free synthesis of alkynyl alkyl selenides via three-component coupling of terminal alkynes, Se, and epoxides

2018 ◽  
Vol 20 (7) ◽  
pp. 1560-1563 ◽  
Author(s):  
Ge Wu ◽  
Lin Min ◽  
Hongchen Li ◽  
Wenxia Gao ◽  
Jinchang Ding ◽  
...  
Keyword(s):  
Formation Process ◽  
Bond Formation ◽  
Coupling Reaction ◽  
Terminal Alkynes ◽  
Metal Free ◽  
Three Component Coupling

A metal-free three-component coupling reaction of alkynes, Se powder and epoxides is described, providing an efficient, straightforward route for the preparation of alkynyl alkyl selenides via a double C–Se bond formation process.

scholarly journals K2S2O8-Promoted Aryl Thioamides Synthesis from Aryl Aldehydes Using Thiourea as the Sulfur Source

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2225 ◽  
Author(s):  
Yongjun Bian ◽  
Xingyu Qu ◽  
Yongqiang Chen ◽  
Jun Li ◽  
Leng Liu
Keyword(s):  
Transition Metal ◽  
Functional Groups ◽  
Sulfur Atom ◽  
Coupling Reaction ◽  
Sulfur Source ◽  
Atom Transfer ◽  
Free Condition ◽  
Metal Free ◽  
Aryl Aldehydes ◽  
Three Component Coupling

Thiourea as a sulfur atom transfer reagent was applied for the synthesis of aryl thioamides through a three-component coupling reaction with aryl aldehydes and N,N-dimethylformamide (DMF) or N,N-dimethylacetamide (DMAC). The reaction could tolerate various functional groups and gave moderate to good yields of desired products under the transition-metal-free condition.

Metal-Free Decarboxylative Three-Component Coupling Reaction for the Synthesis of Propargylamines

2013 ◽  
Vol 15 (13) ◽  
pp. 3322-3325 ◽  
Author(s):  
Kyungho Park ◽  
Yumi Heo ◽  
Sunwoo Lee
Keyword(s):  
Coupling Reaction ◽  
Metal Free ◽  
Three Component Coupling

ChemInform Abstract: NH4I-Mediated Three-Component Coupling Reaction: Metal-Free Synthesis of β-Alkoxy Methyl Sulfides from DMSO, Alcohols, and Styrenes.

ChemInform ◽  
2015 ◽  
Vol 46 (28) ◽  
pp. no-no
Author(s):  
Xiaofang Gao ◽  
Xiaojun Pan ◽  
Jian Gao ◽  
Huanfeng Jiang ◽  
Gaoqing Yuan ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Metal Free ◽  
Three Component Coupling

NH4I-Mediated Three-Component Coupling Reaction: Metal-Free Synthesis of β-Alkoxy Methyl Sulfides from DMSO, Alcohols, and Styrenes

2015 ◽  
Vol 17 (4) ◽  
pp. 1038-1041 ◽  
Author(s):  
Xiaofang Gao ◽  
Xiaojun Pan ◽  
Jian Gao ◽  
Huanfeng Jiang ◽  
Gaoqing Yuan ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Metal Free ◽  
Three Component Coupling

Metal-Free Three-Component Coupling Reaction of Ketones with Electron-rich Arenes and Selenium Dioxide for the Synthesis of α-Arylselanyl Ketones

2020 ◽  
Vol 85 (23) ◽  
pp. 15652-15659
Author(s):  
Kmendashisha Wanniang ◽  
O. Risuklang Shangpliang ◽  
Ibakyntiew D. Marpna ◽  
Tyrchain Mitre Lipon ◽  
Badaker M. Laloo ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Selenium Dioxide ◽  
Metal Free ◽  
Three Component Coupling

Visible light-induced alkylpyridylation of styrenes via a reductive radical three-component coupling

2021 ◽  
Author(s):  
Jingmiao Yu ◽  
Liwen Zhu ◽  
Huan Gao ◽  
Xiaoyuan Hong ◽  
Tingting Chen
Keyword(s):  
Visible Light ◽  
Coupling Reaction ◽  
Metal Free ◽  
Radical Coupling ◽  
Radical Coupling Reaction ◽  
Three Component Coupling

A visible light-induced and metal-free strategy for the intermolecular three-compoment alkylpyridylation of styrenes is reported. Hantzsch ester was found to be key to initiate the overall reductive radical coupling reaction....

scholarly journals N-Alkylation/aldol reaction of α-aldimino thioesters: a facile three-component coupling reaction

RSC Advances ◽  
2021 ◽  
Vol 11 (22) ◽  
pp. 13097-13104
Author(s):  
Makoto Shimizu ◽  
Asako Higashino ◽  
Isao Mizota ◽  
Yusong Zhu
Keyword(s):  
Aldol Reaction ◽  
Coupling Reaction ◽  
Three Component Coupling

Treatment of α-aldimino thioesters with dialkylzinc reagents in the presence of aldehydes or imines gives three-component coupling products in good yields with good to high anti-selectivities.

Sign in / Sign up

Export Citation Format

Share Document