A Novel Synthesis of N-Substituted 2-(Benzotriazol-1-yl)acetamides Promoted by Samarium Diiodide.

ChemInform ◽  
2003 ◽  
Vol 34 (14) ◽  
Author(s):  
Weike Su ◽  
Bibo Yang ◽  
Yongshu Li
Keyword(s):  
Samarium Diiodide ◽  
Novel Synthesis

Samarium Diiodide Induced Reductive Cleavage of the Se–Se Bond in Diselenides: A Novel Synthesis of 3-Substituted-Imidazolidine-2-One-1-Carbonyl Selenoesters

2002 ◽  
Vol 2002 (4) ◽  
pp. 168-169 ◽  
Author(s):  
Weike Su ◽  
Ning Gao ◽  
Yongmin Zhang
Keyword(s):  
Reductive Cleavage ◽  
Samarium Diiodide ◽  
Novel Synthesis ◽  
Neutral Conditions ◽  
Substituted 1

The reduction of diselenides by samarium diiodide led to samarium selenolates (RSeSmI2). These species reacted with 3-substituted-1-chlorocarbonyl-imidazolidin-2-ones to give the corresponding selenoesters in good yields under mild and neutral conditions.

A Novel Synthesis of N-substituted 2-(benzotriazol-1-yl) Acetamides Promoted by Samarium Diiodide

2002 ◽  
Vol 2002 (11) ◽  
pp. 542-543 ◽  
Author(s):  
Weike Su ◽  
Bibo Yang ◽  
Yongshu Li
Keyword(s):  
Samarium Diiodide ◽  
Novel Synthesis ◽  
Neutral Conditions

1-(Chloromethyl)benzotriazole undergo reaction with isocyanates promoted by samarium diiodide to afford N-substituted 2-(benzotriazol-1-yl)acetamides in good yields under mild and neutral conditions.

Novel Synthesis of CIF6+ and BrF6+

2000 ◽  
Author(s):  
Thorsten Schroer ◽  
Karl O. Christe
Keyword(s):  
Novel Synthesis
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