A Carbon-Carbon Bond Formation by the Reaction of 4-Chloro-6-methyl-3-phenylethynyl-2H-pyran-2-one with Active Methylene Derivatives

Heterocycles ◽  
1996 ◽  
Vol 42 (2) ◽  
pp. 789 ◽  
Author(s):  
Yutaka Azuma ◽  
Atsuko Sato ◽  
Mieko Morone
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Active Methylene

scholarly journals Mild polyaddition and polyalkylation based on the carbon–carbon bond formation reaction of active methylene

RSC Advances ◽  
2019 ◽  
Vol 9 (69) ◽  
pp. 40455-40461
Author(s):  
Caicai Jiao ◽  
Lilong Gao ◽  
Bing Yu ◽  
Hailin Cong ◽  
Youqing Shen
Keyword(s):  
High Throughput ◽  
Bond Formation ◽  
Formation Reaction ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Active Methylene

Active methylene-based polyaddition and polyalkylation catalyzed via an organic superbase were studied in a high-throughput parallel synthesizing instrument.

Carbon-carbon bond formation from ethyl cyanoformate and active methylene compounds

1979 ◽  
Vol 20 (27) ◽  
pp. 2525-2528 ◽  
Author(s):  
Takamasa Iimori ◽  
Yasushi Nii ◽  
Toshio Izawa ◽  
Susumu Kobayashi ◽  
Masaji Ohno
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Active Methylene Compounds ◽  
Active Methylene

Manganese(III)-mediated carbon-carbon bond formation in the reaction of xanthenes with active methylene compounds

1992 ◽  
Vol 57 (13) ◽  
pp. 3551-3557 ◽  
Author(s):  
Hiroshi Nishino ◽  
Hironori Kamachi ◽  
Harumi Baba ◽  
Kazu Kurosawa
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Active Methylene Compounds ◽  
Active Methylene

Carbon Dioxide-Mediated C(sp2)–H Arylation of Primary and Secondary Benzylamines

2018 ◽  
Author(s):  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Michael Young
Keyword(s):  
Carbon Dioxide ◽  
Transition Metal ◽  
Bond Activation ◽  
Bond Formation ◽  
Carbon Bond ◽  
Chelate Effect ◽  
Free Amine ◽  
Carbon Carbon Bond ◽  
New Strategy ◽  
Metal Catalyzed

Carbon-carbon bond formation by transition metal-catalyzed C–H activation has become an important strategy to fabricate new bonds in a rapid fashion. Despite the pharmacological importance of <i>ortho</i>-arylbenzylamines, however, effective <i>ortho</i>-C–C bond formation from C–H bond activation of free primary and secondary benzylamines using Pd<sup>II</sup> remains an outstanding challenge. Presented herein is a new strategy for constructing <i>ortho</i>-arylated primary and secondary benzylamines mediated by carbon dioxide (CO<sub>2</sub>). The use of CO<sub>2</sub> is critical to allowing this transformation to proceed under milder conditions than previously reported, and that are necessary to furnish free amine products that can be directly used or elaborated without the need for deprotection. In cases where diarylation is possible, a chelate effect is demonstrated to facilitate selective monoarylation.

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