Highly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C−H Bond Activation

2004 ◽  
Vol 126 (23) ◽  
pp. 7192-7193 ◽  
Author(s):  
Reema K. Thalji ◽  
Jonathan A. Ellman ◽  
Robert G. Bergman
Keyword(s):  
Bond Activation ◽  
Highly Efficient ◽  
Aromatic Imines

scholarly journals Highly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C—H Bond Activation.

ChemInform ◽  
2004 ◽  
Vol 35 (42) ◽  
Author(s):  
Reema K. Thalji ◽  
Jonathan A. Ellman ◽  
Robert G. Bergman
Keyword(s):  
Bond Activation ◽  
Highly Efficient ◽  
Aromatic Imines

C–H Bond Activation by σ-Bond Metathesis as a Versatile Route toward Highly Efficient Initiators for the Catalytic Precision Polymerization of Polar Monomers

2015 ◽  
Vol 34 (11) ◽  
pp. 2703-2706 ◽  
Author(s):  
Benedikt S. Soller ◽  
Stephan Salzinger ◽  
Christian Jandl ◽  
Alexander Pöthig ◽  
Bernhard Rieger
Keyword(s):  
Bond Activation ◽  
Highly Efficient ◽  
Polar Monomers

scholarly journals Annulation of Aromatic Imines via Directed C—H Bond Activation.

ChemInform ◽  
2005 ◽  
Vol 36 (52) ◽  
Author(s):  
Reema K. Thalji ◽  
Kateri A. Ahrendt ◽  
Robert G. Bergman ◽  
Jonathan A. Ellman
Keyword(s):  
Bond Activation ◽  
Aromatic Imines

ChemInform Abstract: Asymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C—H Bond Activation.

ChemInform ◽  
2008 ◽  
Vol 39 (5) ◽  
Author(s):  
Anja Watzke ◽  
Rebecca M. Wilson ◽  
Steven J. O'Malley ◽  
Robert G. Bergman ◽  
Jonathan A. Ellman
Keyword(s):  
Bond Activation ◽  
Intramolecular Alkylation ◽  
Aromatic Imines

Ru(ii)/PEG-400 as a highly efficient and recyclable catalytic media for annulation and olefination reactions via C–H bond activation

2016 ◽  
Vol 18 (20) ◽  
pp. 5635-5642 ◽  
Author(s):  
Subhash L. Yedage ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Bond Activation ◽  
Weinreb Amides ◽  
Peg 400 ◽  
Highly Efficient ◽  
Olefination Reactions

In this report synthesis of isoquinolinones, isocoumarins, and N-methyl isoquinolinones and olefination of Weinreb amides by C–H bond activation using Ru(ii)/PEG-400 as green and recyclable media are documented.

Nickel-Catalyzed Decarbonylative Thioetherification of Acyl Fluorides via C-F Bond Activation

Synthesis ◽  
2021 ◽  
Author(s):  
Jingwen You ◽  
Qiang Chen ◽  
Yasushi Nishihara
Keyword(s):  
Functional Groups ◽  
Bond Activation ◽  
Highly Efficient ◽  
Wide Range

Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon-sulfur bonds via a highly efficient decarbonylative process.

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