pHarmacist (pHantasticant) 11-22-03 23:57 No 472576 |
A new approach to the ergoline skeleton (Rated as: good read) |
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Tetrahedron 59 (2003) 4281–4286 (http://pharmacist-hive.tripod.com/ergol Mária Incze, István Moldvai, Eszter Temesvári-Major, Gábor Dörnyei, Mária Kajtár-Peredy and Csaba Szántay Abstract: Starting from N-pivaloyl-Uhle's ketone a new synthetic approach to the ergoline skeleton has been elaborated. Ring D of the tetracyclic skeleton was formed by an intramolecular Dieckmann-condensation of a diester, obtained in a Reformatsky reaction of a properly substituted derivative of N-pivaloyl Uhle's ketone followed by elimination of water. http://www.bassdrive.com/BassDrive.m3u |
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