A simple and convenient method for the preparation of diborane from tetrabutylammonium borohydride and benzyl chloride for application in organic synthesis
A simple and convenient method for the preparation of diborane from tetrabutylammonium borohydride and benzyl chloride for application in organic synthesis
| dc.contributor.author | Periasamy, Mariappan | |
| dc.contributor.author | Muthukumaragopal, G. P. | |
| dc.contributor.author | Sanjeevakumar, Nalluri | |
| dc.date.accessioned | 2022-03-27T09:08:12Z | |
| dc.date.available | 2022-03-27T09:08:12Z | |
| dc.date.issued | 2007-09-24 | |
| dc.description.abstract | Diborane is readily generated in situ at 25 °C in toluene using the Bu4NBH4/PhCH2Cl and Bu4NBH4/I2 reagent systems. The reagent prepared in this way is used for the reduction of carbonyl compounds and hydroboration-oxidation of olefins to obtain the corresponding alcohols in good yields. © 2007 Elsevier Ltd. All rights reserved. | |
| dc.identifier.citation | Tetrahedron Letters. v.48(39) | |
| dc.identifier.issn | 00404039 | |
| dc.identifier.uri | 10.1016/j.tetlet.2007.07.173 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0040403907015031 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12473 | |
| dc.subject | Hydroboration | |
| dc.subject | Oxidation | |
| dc.subject | Reduction | |
| dc.subject | Tetrabutylammonium borohydride | |
| dc.title | A simple and convenient method for the preparation of diborane from tetrabutylammonium borohydride and benzyl chloride for application in organic synthesis | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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