Synthesis, Inhaltsverzeichnis PAPER© Georg Thieme Verlag Stuttgart · New YorkSynthesis of Homo- and HeterobiarylmethylaminesVincent Terrasson, Sylvain Marque, Annabelle Scarpacci, Damien Prim*Université de Versailles, Insitut Lavoisier, UMR CNRS 8180, 45, avenue des Etats-Unis, 78035 Versailles Cedex, France Fax: +33(1)39254452; e-Mail: prim@chimie.uvsq.fr; Artikel empfehlen Abstract Artikel einzeln kaufen(opens in new window) Alle Artikel dieser Rubrik(opens in new window) Abstract A variety of homo- and heterobiarylmethylamines were prepared in modest to high yields via a convenient one-pot process. Key words biarylmethylamines - imines - nitriles - nucleophilic addition Volltext Referenzen References <A NAME="RZ02006SS-1">1</A> Bolshan Y. Batey RA. Org. Lett. 2005, 7: 1481 <A NAME="RZ02006SS-2">2</A> Calderon SN. Rothman RB. Porreca F. Flippen-Anderson JL. McNutt RW. Xu H. Smith LE. Bilsky EJ. Davis P. Rice KC. J. Med. Chem. 1994, 37: 2125 <A NAME="RZ02006SS-3A">3a</A> Gil-Molto J. Karlström S. Najera C. Tetrahedron 2005, 61: 12168 <A NAME="RZ02006SS-3B">3b</A> Najera C. Gil-Molto J. Karlström S. Falvello LR. Org. Lett. 2003, 5: 1451 <A NAME="RZ02006SS-3C">3c</A> Silberg J. Schareina T. Kempe R. Wurst K. Buchmeiser MR. J. Organomet. Chem. 2001, 622: 6 <A NAME="RZ02006SS-4">4</A> Arnold PJ. Davies SC. Dilworth JR. Durrant MC. Griffiths DV. Hughes DL. Richards RL. Sharpe PC. J. Chem. Soc., Dalton Trans. 2001, 736 <A NAME="RZ02006SS-5">5</A> Chang J. Plummer S. Berman ESF. Striplin D. Blauch D. Inorg. Chem. 2004, 43: 1735 <A NAME="RZ02006SS-6">6</A> Ligtenbarg AGJ. Spek AL. Hage R. Feringa BL. J. Chem. Soc., Dalton Trans. 1999, 659 See, for example: <A NAME="RZ02006SS-7A">7a</A> van den Heuvel M. van den Berg TA. Kellog RM. Choma CT. Feringa BL. J. Org. Chem. 2004, 69: 250 <A NAME="RZ02006SS-7B">7b</A> Choma CT. Schudde EP. Kellog RM. Robillard GT. Feringa BL. J. Chem. Soc., Perkin Trans. 1 1998, 769 ; and references cited therein See, for example: <A NAME="RZ02006SS-8A">8a</A> Dejaegher Y. Mangelinckx S. De Kimpe N. Synlett 2001, 113 <A NAME="RZ02006SS-8B">8b</A> Weiberth FJ. Hall SS. J. Org. Chem. 1986, 51: 5338 <A NAME="RZ02006SS-9A">9a</A> Bluhm ME. Ciesielski M. Gorls H. Doring M. Angew. Chem. Int. Ed. 2002, 41: 2962 <A NAME="RZ02006SS-9B">9b</A> Renz M. Hemmert C. Meunier B. Eur. J. Org. Chem. 1998, 1271 <A NAME="RZ02006SS-9C">9c</A> Niemers E. Hiltmann R. Synthesis 1976, 593 <A NAME="RZ02006SS-10A">10a</A> In some cases, the use of additives such as CuBr has been described. See ref. 8b. <A NAME="RZ02006SS-10B">10b</A> See also: Weiberth FJ. Hall SS. J. Org. Chem. 1987, 52: 3901 <A NAME="RZ02006SS-11A">11a</A> Compound 6 has already been observed under similar conditions: Grosjean B. Compagnon P.-L. Bull. Soc. Chim. Fr. 1975, 775 <A NAME="RZ02006SS-11B">11b</A> In case of pyridine substrates, ring opening by-products have also been observed: Strekowski L. Watson RA. Faunce MA. Synthesis 1987, 579