ARTICLE;
CATALYSIS;
CHEMICAL REACTION;
CHROMATOGRAPHY;
GAS CHROMATOGRAPHY;
HIGH TEMPERATURE PROCEDURES;
HYDROLYSIS;
INFRARED RADIATION;
NUCLEAR MAGNETIC RESONANCE;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PRIORITY JOURNAL;
For monographs, see: (a). Academic, London. Wiley, New York. E.W. Abel, F.G.A. Stone, G. Wilkinson, & A. McKillop. Pergamon, Oxford. Oxford: Pergamon
For monographs, see: (a) Wakefield B.J. Organolithium Methods. 1988;Academic, London, (b) Sapse A.M., von Ragué Schleyer P. Lithium Chemistry: A Theoretical and Experimental Overview. 1995;Wiley, New York, (c) Gray M., Tinkel M., Sniekus V. Abel E.W., Stone F.G.A., Wilkinson G., McKillop A. Comprehensive Organometallic Chemistry II. Vol. 11:1995;1-92 Pergamon, Oxford, (d) Clayden J. Organolithiums: Selectivity for Synthesis. 2002;Pergamon, Oxford.
For reviews, see: (a) Yus M. Chem. Soc. Rev. 25:1996;155-161 (b) Ramón D.J., Yus M. Eur. J. Org. Chem. 2000;225-237 (c) Yus M. Synlett. 2001;1197-1205 (d) Yus M., Ramón D.J. Lat. J. Chem. 2002;79-92 (e) Ramón D.J., Yus M. Rev. Cubana Quim. 14:2002;75-115.
For polymer versions of this reaction, see: (a) Gómez C., Ruiz S., Yus M. Tetrahedron Lett. 39:1998;1397-1400 (b) Gómez C., Ruiz S., Yus M. Tetrahedron. 55:1999;7017-7026 (c) Yus M., Candela P., Gómez C. Tetrahedron. 58:2002;6207-6210 (d) Arnauld T., Barret A.G.M., Hopkins B.T. Tetrahedron Lett. 43:2002;1081-1083.
(a) Ramón D.J., Yus M. Tetrahedron Lett. 33:1992;2217-2220 (b) Gómez C., Ramón D.J., Yus M. Tetrahedron. 49:1993;4117-4126 (c) Alonso F., Lorenzo E., Yus M. Tetrahedron Lett. 38:1997;2187-2190 (d) Alonso F., Lorenzo E., Yus M. Tetrahedron Lett. 39:1998;3303-3306 (e) Alonso F., Falvello L.R., Fanwick P.E., Lorenzo E., Yus M. Synthesis. 2000;949-952 (f) Lorenzo E., Alonso F., Yus M. Tetrahedron. 56:2000;469-482.
For a monograph, see: (a). Berlin: Springer. For a review, see: (b)
For a monograph, see: (a) Blomberg C. The Barbier Reaction and Related Processes. 1993;Springer, Berlin. For a review, see: (b) Alonso F., Yus M. Recent. Res. Dev. Org. Chem. 1:1997;397-436.
One of the referees pointed out that the reaction with dicyclopropyl ketone (Table, entry 9) rules out a mechanism involving double ketyl SN2′ addition to the double bond with displacement of halide that could explain the formation of the obtained products. We thank the referee for this observation
One of the referees pointed out that the reaction with dicyclopropyl ketone (Table, entry 9) rules out a mechanism involving double ketyl SN2′ addition to the double bond with displacement of halide that could explain the formation of the obtained products. We thank the referee for this observation.
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For reviews, see: (a)
For reviews, see: (a) Nájera C., Yus M. Trends Org. Chem. 2:1991;155-181 (b) Nájera C., Yus M. Recent Res. Devel. Org. Chem. 1:1997;67-96 (c) Yus M., Foubelo F. Rev. Heteroat. Chem. 17:1997;73-107 (d) Boudier A., Bromm L.O., Lotz M., Knochel P. Angew. Chem. Int. Ed. 39:2000;4414-4435 (e) Nájera C., Yus M. Curr. Org. Chem. 7:2003;867-926.