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- Ruthenium Olefin Metathesis Catalysts Featuring a Labile.
- Ring Closing Metathesis (RCM).
Mauduit, J. Pd, Ru, and Fe catalysis enable a general synthesis of 2-substituted pyrroles in overall good yields with only water and ethene as side-products. The route starts with two subsequent Pd-catalyzed monoallylations of amines with allylic alcohols. Ru-catalyzed ring-closing metathesis performed on the diallylated amines provides pyrrolines in excellent yields. By addition of ferric chloride, a selective aromatization was achieved. Bunrit, S.
Mechanism and activity of ruthenium olefin metathesis catalysts. - Dimensions
Sawadjoon, S. Samec, J. Chen, Z. Zhang, M. Ma, C. Zhong, S. Lee, Org. Wakamatsu, Y. Saito, M. Masubuchi, R.
Fujita, Synlett , , Castarlenas, C. Vovard, C. Fischmeister, P. Dixneuf, J. Bieniek, R. Bujok, M. Cabaj, N. Lugan, G. Lavigne, D. Arlt, K. Lipshutz, S. Sanford M. Mechanism and activity of ruthenium olefin metathesis catalysts. Although the mechanism of 1st generation ruthenium metathesis catalysts had been explored in a number … [Continue reading].
Farina, V. Process Res. Flook, M. Z-Selective olefin metathesis processes catalyzed by a molybdenum hexaisopropylterphenoxide monopyrrolide complex. A , , Tetrahedron , 65 , Organometallics , 26, Graf, M. Loboda, O. Fullerenes Nanotubes and Carbon Nanostructures , 14 , Part II. C-H Activation by Oxidative Addition. Lillehaug, S. Jensen, V. Macromolecules , 38 , Chemphyschem , 6 , A question of coordination.
Teigen, K. Pteridines , 16 , Wendt, R. Organometallics , 20 , Phosphinoalkyl-substituted systems. Angermund, K. Organometallics , 19 , Rapid Commun.
Ystenes, B. A computational study. Insertion of ethylene into a titanium-carbon bond. Journal of Molecular Modeling , 3 ,
Related mechanism and activity of ruthenium olefin metathesis catalysts
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