scholarly journals Ruthenium-Catalyzed Carbon—Carbon Bond Formation Between Propargylic Alcohols and Alkenes via the Allenylidene-Ene Reaction.

ChemInform ◽  
2003 ◽  
Vol 34 (37) ◽  
Author(s):  
Yoshiaki Nishibayashi ◽  
Youichi Inada ◽  
Masanobu Hidai ◽  
Sakae Uemura
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Ene Reaction ◽  
Propargylic Alcohols ◽  
Carbon Carbon Bond

Novel Carbon−Carbon Bond Formation from Propargylic Alcohols and Olefin toward Five-Membered Heterocyclic Rings Catalyzed by AgSbF6

2009 ◽  
Vol 11 (15) ◽  
pp. 3206-3209 ◽  
Author(s):  
Ke-Gong Ji ◽  
Xing-Zhong Shu ◽  
Shu-Chun Zhao ◽  
Hai-Tao Zhu ◽  
Yan-Ning Niu ◽  
...  
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Propargylic Alcohols ◽  
Carbon Carbon Bond

ChemInform Abstract: Novel Carbon-Carbon Bond Formation from Propargylic Alcohols and Olefin Toward Five-Membered Heterocyclic Rings Catalyzed by AgSbF6.

ChemInform ◽  
2009 ◽  
Vol 40 (48) ◽  
pp. no-no
Author(s):  
Ke-Gong Ji ◽  
Xing-Zhong Shu ◽  
Shu-Chun Zhao ◽  
Hai-Tao Zhu ◽  
Yan-Ning Niu ◽  
...  
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Propargylic Alcohols ◽  
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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