| Literature DB >> 20726566 |
Sean M A Kedrowski1, Dennis A Dougherty.
Abstract
The reductive deoxygenation of acyl phosphonates using a Wolff-Kishner-like sequence is described. This transformation allows direct access to alkyl phosphonates from acyl phosphonates at room temperature. The method can be combined with acyl phosphonate synthesis into a one pot, four-step procedure for the conversion of carboxylic acids into alkyl phosphonates. The methodology works well for a variety of aliphatic acids and shows a functional group tolerance similar to that of other hydrazone-forming reactions.Entities:
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Year: 2010 PMID: 20726566 PMCID: PMC2941390 DOI: 10.1021/ol1015493
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005