scholarly journals Formic Acid Reduction. X. Reductive Fission of Bridged Carbon-Carbon Bond of Bisdimedone Derivatives

1971 ◽  
Vol 19 (8) ◽  
pp. 1540-1545 ◽  
Author(s):  
MINORU SEKIYA ◽  
KUNIO SUZUKI
Keyword(s):  
Formic Acid ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Acid Reduction

Hydrothermal Carbon−Carbon Bond Formation and Disproportionations of C1 Aldehydes:  Formaldehyde and Formic Acid

2005 ◽  
Vol 109 (29) ◽  
pp. 6610-6619 ◽  
Author(s):  
Saiko Morooka ◽  
Chihiro Wakai ◽  
Nobuyuki Matubayasi ◽  
Masaru Nakahara
Keyword(s):  
Formic Acid ◽  
Bond Formation ◽  
Carbon Bond ◽  
Carbon Carbon Bond

scholarly journals Direct conversion of glycerol into formic acid via water stable Pd(II) catalyzed oxidative carbon–carbon bond cleavage

2013 ◽  
Vol 54 (33) ◽  
pp. 4463-4466 ◽  
Author(s):  
Prasanna Pullanikat ◽  
Joo Ho Lee ◽  
Kyung Soo Yoo ◽  
Kyung Woon Jung
Keyword(s):  
Formic Acid ◽  
Bond Cleavage ◽  
Direct Conversion ◽  
Carbon Bond ◽  
Carbon Carbon Bond

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.

Modern Organic Synthesis in the Laboratory

2008 ◽  
Author(s):  
Jie Jack Li ◽  
Chris Limberakis ◽  
Derek A. Pflum
Keyword(s):  
Organic Chemistry ◽  
Graduate Students ◽  
Organic Synthesis ◽  
Functional Group ◽  
Bond Formation ◽  
Reaction Conditions ◽  
Carbon Bond ◽  
Oxidation Reduction ◽  
Carbon Carbon Bond ◽  
Daunting Task

Searching for reaction in organic synthesis has been made much easier in the current age of computer databases. However, the dilemma now is which procedure one selects among the ocean of choices. Especially for novices in the laboratory, it becomes a daunting task to decide what reaction conditions to experiment with first in order to have the best chance of success. This collection intends to serve as an "older and wiser lab-mate" one could have by compiling many of the most commonly used experimental procedures in organic synthesis. With chapters that cover such topics as functional group manipulations, oxidation, reduction, and carbon-carbon bond formation, Modern Organic Synthesis in the Laboratory will be useful for both graduate students and professors in organic chemistry and medicinal chemists in the pharmaceutical and agrochemical industries.

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