Nickel-catalyzed hydrogenolysis of unactivated carbon-cyano bonds
DSpace at IIT Bombay
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Title |
Nickel-catalyzed hydrogenolysis of unactivated carbon-cyano bonds
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Creator |
PATRA, T
AGASTI, S MODAK, A MAITI, D |
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Subject |
C-CN BOND
TRANSITION-METAL COMPLEX REDUCTIVE CLEAVAGE ARYL ETHERS O BONDS INTRAMOLECULAR ARYLCYANATION PALLADIUM CATALYST DIRECT CONVERSION DIRECTING GROUPS IRON-COMPLEX |
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Description |
Selective hydrogenolysis of C-CN bonds can allow chemists to take advantage of ortho-directing ability, alpha-C-H acidity and electron withdrawing ability of the cyano group for synthetic manipulations. We have discovered hydrogenolysis of aryl and aliphatic cyanides under just 1 bar of hydrogen by using a nickel catalyst. This protocol was applied in the aryl cyanide directed functionalization reaction and alpha-substitution of benzyl cyanides.
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Publisher |
ROYAL SOC CHEMISTRY
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Date |
2014-10-15T13:09:10Z
2014-10-15T13:09:10Z 2013 |
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Type |
Article
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Identifier |
CHEMICAL COMMUNICATIONS, 49(75)8362-8364
1359-7345 1364-548X http://dx.doi.org/10.1039/c3cc44562c http://dspace.library.iitb.ac.in/jspui/handle/100/14967 |
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Language |
en
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