2,5,6-Trisubstituted N-methylindoles from site-selective Suzuki-Miyaura cross-coupling, twofold Heck and 6π-electrocyclization-dehydrogenation reactions of 2,3,5-tribromo-N-methylpyrrole
Site-selective Suzuki-Miyaura reactions of 2,3,5-tribromo-N-methylpyrrole afforded 5-aryl-2,3-dibromo-N-methylpyrroles. These products were transformed into 2,5,6-trisubstituted N-methylindoles by twofold Heck reactions and subsequent 6π-electrocyclizatio
Toguem, Serge-Mithérand Tengho,Langer, Peter
p. 513 - 516
(2011/04/18)
More Articles about upstream products of 1307229-52-2