Synthesis, Table of Contents SHORTPAPER © Georg Thieme Verlag Stuttgart · New York New General One-Pot Synthesis of 1-Alkoxy Cyclic Phosphine Derivatives Graziano Baccolini*, Carla Boga, Rezio A. BuscaroliDipartimento di Chimica Organica ”A. Mangini", Università di Bologna, Viale Risorgimento 4, 40136 Bologna, ItalyFax: +39(51)6443654; e-Mail: baccolin@ms.fci.unibo.it; Recommend Article Abstract Buy Article All articles of this category Abstract Treatment, at room temperature, of benzothiadiphosphole 1 with bis-Grignard 2, sodium alcoholate and finally with S8 afforded 1-alkoxy cyclic phosphine sulfides in good yields. In a similar manner, reactions with sodium phenylthiolate gave the corresponding 1-phenylsulfanyl cyclic phosphine derivatives. Key words phosphorus - heterocycles - Grignard reactions - cyclizations - 1-alkoxy cyclic phosphine sulfides Full Text References References 1a Baccolini G. Mezzina E. Todesco PE. Foresti E. J. Chem. Soc., Chem. Commun. 1988, 304 1b Baccolini G. Beghelli M. Boga C. Heteroat. Chem. 1997, 8: 551 1c Gang Wu R. Wasylishen E. Power WP. Baccolini G. Can. J. Chem. 1992, 72: 1229 2 Baccolini G. Orsolan G. Mezzina E. Tetrahedron Lett. 1995, 36: 447 3 Baccolini G. Boga C. Negri U. Synlett 2000, 1685 For reviews on pentacoordinated and hexacoordinated phosphorus, see: 4a Holmes RR. Pentacoordinated Phosphorus Structure and Spectroscopy Vol. I and II: ACS Monograph 175; Washington: 1980. 4b Wong CY. Kennepohl DK. Cavell RG. Chem. Rev. 1996, 96: 1917 4c Holmes RR. Acc. Chem. Res. 1998, 31: 535 5 Holand S. Mathey F. J. Org. Chem. 1981, 46: 4386 6 Niemi TA. Coe PL. Till SJ. J. Chem. Soc., Perkin Trans. 1 2000, 1519 7 Bergbreiter DE. Pendergrass E. J. Org. Chem. 1981, 46: 219