Carbon Dioxide Promoted Palladium-Catalyzed Cyclotrimerization of Alkynes in Water.

ChemInform ◽  
2004 ◽  
Vol 35 (38) ◽  
Author(s):  
Jin-Heng Li ◽  
Ye-Xiang Xie
Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 519-524 ◽  
Author(s):  
Michael Young ◽  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Justin Maxwell ◽  
Daniel Liu ◽  
...  

Amines are an important class of compounds in organic chemistry and serve as an important motif in various industries, including pharmaceuticals, agrochemicals, and biotechnology. Several methods have been developed for the C–H functionalization of amines using various directing groups, but functionalization of free amines remains a challenge. Here, we discuss our recently developed carbon dioxide driven highly site-selective γ-arylation of alkyl- and benzylic amines via a palladium-catalyzed C–H bond-activation process. By using carbon dioxide as an inexpensive, sustainable, and transient directing group, a wide variety of amines were arylated at either γ-sp3 or sp2 carbon–hydrogen bonds with high selectivity based on substrate and conditions. This newly developed strategy provides straightforward access to important scaffolds in organic and medicinal chemistry without the need for any expensive directing groups.1 Introduction2 C(sp3)–H Arylation of Aliphatic Amines3 C(sp2)–H Arylation of Benzylamines4 Mechanistic Questions5 Future Outlook


2011 ◽  
Vol 282 (1) ◽  
pp. 120-127 ◽  
Author(s):  
Nicola Della Ca’ ◽  
Paolo Bottarelli ◽  
Angela Dibenedetto ◽  
Michele Aresta ◽  
Bartolo Gabriele ◽  
...  

2006 ◽  
Vol 299 ◽  
pp. 66-72 ◽  
Author(s):  
Marco Burgener ◽  
Tomasz Tyszewski ◽  
Davide Ferri ◽  
Tamas Mallat ◽  
Alfons Baiker

ChemInform ◽  
2010 ◽  
Vol 33 (6) ◽  
pp. no-no
Author(s):  
Tessa R. Early ◽  
Richard S. Gordon ◽  
Michael A. Carroll ◽  
Andrew B. Holmes ◽  
Richard E. Shute ◽  
...  

2007 ◽  
Vol 9 (19) ◽  
pp. 3817-3820 ◽  
Author(s):  
George E. Greco ◽  
Brittany L. Gleason ◽  
Tiffany A. Lowery ◽  
Matthew J. Kier ◽  
Lisa B. Hollander ◽  
...  

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