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http://nopr.niscpr.res.in/handle/123456789/21661Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ramaiah, K | - |
| dc.contributor.author | Dubey, P K | - |
| dc.contributor.author | Ramanatham, J | - |
| dc.contributor.author | Kumar, C Ravi | - |
| dc.contributor.author | Grossert, J S | - |
| dc.date.accessioned | 2013-10-07T10:30:58Z | - |
| dc.date.available | 2013-10-07T10:30:58Z | - |
| dc.date.issued | 2003-07 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/21661 | - |
| dc.description | 1765-1767 | en_US |
| dc.description.abstract | Benzimidazolium dichromates have been used for the selective and efficient oxidation of simple alcohols to carbonyl compounds. 2-Methylbenzimidazolium dichromate has been used as a standard compound. It has been found to oxidize selectively, primary alcohols to aldehydes, without any over-oxidation, and secondary alcohols to ketones. Of the several solvents explored, acetic acid at RT has been found to be the best medium for oxidation. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.42B(07) [July 2003] | en_US |
| dc.title | Benzimidazolium dichromates : Efficient reagents for selective oxidation of alcohols to carbonyl compounds | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.42B(07) [July 2003] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 42B(7) 1765-1767.pdf | 551.67 kB | Adobe PDF | View/Open |
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