Back to Search Start Over

An efficient one-step chemoselective reduction of alkyl ketones over aryl ketones in β-diketones using LiHMDS and lithium aluminium hydride

Authors :
Veeraswamy, S.
Indrasena Reddy, K.
Venkat Ragavan, R.
Tirumal Reddy, K.
Yennam, Satyanarayana
Jayashree, A.
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Aug2012, Vol. 53 Issue 35, p4651-4653. 3p.
Publication Year :
2012

Abstract

Abstract: β-Hydroxy ketones were synthesized in one-pot from β-diketones by reducing alkyl ketones chemoselectively by keeping aryl ketone intact. Initially, β-diketones were enolized using LiHMDS and later alkyl ketone was chemoselectively reduced efficiently by lithium aluminium hydride. This method produces β- hydroxyl ketones from the corresponding β-diketones in high yield. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
53
Issue :
35
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
78169326
Full Text :
https://doi.org/10.1016/j.tetlet.2012.06.057