Reactions of 1,4,7-trithiacyclononane, [9]aneS3, with early transition metal halides: synthesis and X-ray structure of {Fe([9]aneS3)2}[Sb2Cl8]

1994 ◽  
Vol 19 (2) ◽  
pp. 187-190 ◽  
Author(s):  
Gerald R. Willey ◽  
Janet Palin ◽  
Miles T. Lakin ◽  
Nathaniel W. Alcock
2019 ◽  
Vol 29 (22) ◽  
pp. 1900293 ◽  
Author(s):  
Jialin Lei ◽  
Georgiy Akopov ◽  
Michael T. Yeung ◽  
Jinyuan Yan ◽  
Richard B. Kaner ◽  
...  

2019 ◽  
Author(s):  
Han Hao ◽  
Laurel Schafer

In the presence of a bis-amidate-bis-amido Ti pre-catalyst, an NHC supported Cu acetylide was reacted with <i>p</i>-toluidine to generate a new Cu containing species almost quantitatively. The product was analyzed by NMR spectroscopy and X-ray single crystal diffraction to be a Cu enamide. Preliminary mechanistic studies suggest the reaction follows well accepted [2+2] cycloaddition mechanism for early transition metal catalyzed hydroamination. Furthermore, the reaction is likely to be a direct functionalization of the alkyne moiety of the Cu acetylide.


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