1. Synthesis of 3-aryl-4, 5-dihydro-5-hydroxy-1,2-oxazoles by reaction of substituted benzonitrile oxides with the enolate ion of acetaldehyde
Di Nunno, L., Di Nunno, L., Scilimati, A.
Tetrahedron, 1987, 43(9), pp. 2181–2189
2. Decomposition of arylazides by thf/n-butyllithium-II-isolation of 1-aryl-4,5-dihydro-5-hydroxy-1h-1,2,3-triazoles
Di Nunno, L., Scilimati, A.
Tetrahedron, 1986, 42(14), pp. 3913–3920
3. Regioselective synthesis and side-chain metallation and elaboration of 3-aryl-5-alkylisoxazoles
Di Nunno, L., Scilimati, A., Vitale, P.
Tetrahedron, 2002, 58(13), pp. 2659–2665
4.Kluyveromyces marxianus CBS 6556 growing cells as a new biocatalyst in the asymmetric reduction of substituted acetophenones
Vitale, P., D'Introno, C., Perna, F.M., Perrone, M.G., Scilimati, A.
Tetrahedron Asymmetry, 2013, 24(7), pp. 389–394
5. Effect of the aryl group substituent in the dimerization of 3-arylisoxazoles to syn 2,6-diaryl-3,7-diazatricyclo[4.2.0.02,5]octan-4,8-diones induced by LDA
Di Nunno, L., Vitale, P., Scilimati, A.
Tetrahedron, 2008, 64(49), pp. 11198–11204
Thank you in advance for your reply. Antonio Scilimati
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