ChemInform Abstract: Palladium-tert-Alkyl Isocyanide Catalyzed Intramolecular Bis- Silylation of Vicinally Disubstituted Alkenes.

ChemInform ◽  
2010 ◽  
Vol 27 (1) ◽  
pp. no-no
Author(s):  
M. SUGINOME ◽  
A. MATSUMOTO ◽  
K. NAGATA ◽  
Y. ITO
Keyword(s):  
1985 ◽  
Vol 4 (1) ◽  
pp. 139-142 ◽  
Author(s):  
James L. Farr ◽  
Michael J. Abrams ◽  
Catherine E. Costello ◽  
Alan. Davison ◽  
Stephen J. Lippard ◽  
...  
Keyword(s):  

1969 ◽  
Vol 47 (7) ◽  
pp. 1217-1222 ◽  
Author(s):  
Takeo Saegusa ◽  
Yoshihiko Ito ◽  
Shiro Kobayashi ◽  
Kiwami Hirota ◽  
Nobuyuki Takeda

The reaction of alkyl isocyanide with alcohol to produce alkyl formimidate requires catalysis by metal compounds. The catalysts are classified into two groups. The first group includes metallic copper, and the oxides of copper (Cu (I) and Cu (II)), silver, and mercury, which induce the isocyanide reactions of various alcohols including saturated and unsaturated alcohols and amino-alcohol. The second group catalysts are the chlorides of copper (Cu (I)), silver, zinc, and cadmium, which cause the reactions of isocyanide only with special alcohols having strong coordinating tendencies toward the catalyst, as being exemplified by allyl alcohol and β-N,N-dimethylaminoethanol. Among these catalysts, metallic copper and copper oxides are the most effective and give the products almost quantitatively. The difference in catalyst activity between the two groups of catalysts has been explained by assuming a ternary complex consisting of the catalyst, isocyanide, and alcohol as the site of reaction.


2017 ◽  
Vol 41 (2) ◽  
pp. 85-87 ◽  
Author(s):  
Ghodsyeh Keykha ◽  
Mohammad R. Hosseini-Tabatabaei ◽  
Alireza Hassanabadi

Good yields of six 1H-chromeno[2,3-d]pyrimidine-5-carboxamides were obtained via the two-stage, one-pot reaction of an alkyl isocyanide with the initially formed condensation product of 1,3-dimethyl barbituric acid and a salicylaldehyde under solvent-free conditions at ambient temperature. This procedure has a number of advantages, such as short reaction time and easy work-up. Also, the present method does not involve any hazardous organic solvent.


Biochemistry ◽  
1989 ◽  
Vol 28 (5) ◽  
pp. 2140-2144 ◽  
Author(s):  
Mehul J. Patel ◽  
Richard J. Kassner ◽  
Terrence E. Meyer ◽  
Michael A. Cusanovich

1983 ◽  
Vol 22 (20) ◽  
pp. 2798-2800 ◽  
Author(s):  
Michael J. Abrams ◽  
Alan Davison ◽  
Alun G. Jones ◽  
Catherine E. Costello ◽  
Henrianna Pang

1992 ◽  
Vol 31 (25) ◽  
pp. 5193-5201 ◽  
Author(s):  
Edmund M. Carnahan ◽  
R. Lynn Rardin ◽  
Simon G. Bott ◽  
Stephen J. Lippard

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