| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1325411 | Journal of Organometallic Chemistry | 2009 | 11 Pages |
A number of novel and synthetically important pyridyl/naphthyl/(diphenyl)methylseleno substituted alkanoic acids (20–25) have been synthesized using an efficient and operationally simple strategy. Starting substrates, ethyl pyridyl/naphthyl/(diphenyl)methylseleno substituted alkanoates (8–13) were easily prepared by treatment of ethyl chloroalkanoates 7(a–c) with nucleophilic selenium reagent RSeNa+, generated from the cleavage of dipyridyl/dinaphthyl/bis(diphenylmethyl) diselenide (1–6) with sodium borohydride in ethanol. The ethyl pyridyl/naphthyl/(diphenyl)methylseleno substituted alkanoates (8–13) on basic hydrolysis and subsequent acidification afford pyridyl/naphthyl/(diphenyl) methylseleno substituted alkanoic acids (20–25) in excellent yields. These selenoalkanoates (8–13) and selenoalkanoic acids (20–25) have been characterized by elemental analysis and various spectroscopic techniques viz. NMR (1H, 13C and 77Se), IR and mass spectrometry. The molecular structure of 2-pyridylselenoethanoic acid (20a), 2-naphthylselenoethanoic acid (23a) and 2-(diphenyl)methylselenoethanoic acid (24a) has also been established with the help of single crystal X-ray analysis.
Graphical abstractA number of novel and synthetically important pyridyl/naphthyl/(diphenyl)methylseleno substituted alkanoic acids have been synthesized by basic hydrolysis and subsequent acidification of ethyl pyridyl/naphthyl/(diphenyl)methylseleno substituted alkanoates, which were conveniently prepared from ethyl chloroalkanoates and dipyridyl/dinaphthyl/bis(diphenylmethyl) diselenide using sodium borohydride in ethanol. The molecular structures of 2-pyridyl/naphthyl/(diphenyl)methyl selenoethanoic acid have been established through X-ray crystallography.Figure optionsDownload full-size imageDownload as PowerPoint slide
