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2002 1
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2007 1
2012 2
2022 0
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Study of the lithiated phenylacetonitrile monoanions and dianions formed according to the lithiated base used (LHMDS, LDA, or n-BuLi). 2. Alkylation and deuteriation mechanism study by vibrational and NMR spectroscopy and quantum chemistry calculations.
Strzalko T, Wartski L, Corset J, Castellà-Ventura M, Froment F. Strzalko T, et al. Among authors: castella ventura m. J Org Chem. 2012 Aug 3;77(15):6431-42. doi: 10.1021/jo300758g. Epub 2012 Jul 23. J Org Chem. 2012. PMID: 22742856
Identification of the monoanions and of their complexes with lithium salts possibly formed in solution during the alkylation of lithiated phenylacetonitrile dianions: infrared spectroscopy and density functional theory calculations.
Corset J, Castellà-Ventura M, Froment F, Strzalko T, Wartski L. Corset J, et al. Among authors: castella ventura m. Spectrochim Acta A Mol Biomol Spectrosc. 2007 Dec 31;68(5):1340-6. doi: 10.1016/j.saa.2007.02.014. Epub 2007 Feb 23. Spectrochim Acta A Mol Biomol Spectrosc. 2007. PMID: 17466572
Structural and vibrational characterization of the mono and dilithiated species derived from phenylacetonitrile in THF by infrared and Raman spectroscopy and density functional theory calculations.
Corset J, Castellà-Ventura M, Froment F, Strzalko T, Wartski L. Corset J, et al. Among authors: castella ventura m. Spectrochim Acta A Mol Biomol Spectrosc. 2002 Jul;58(9):1971-86. doi: 10.1016/s1386-1425(01)00648-5. Spectrochim Acta A Mol Biomol Spectrosc. 2002. PMID: 12164496