Kirchberg S, Frohlich R, Studer A
Forschungsartikel (Zeitschrift)Excellent stereoselectivity is obtained in the synthesis of biologically interesting 1,2,3-trisubstituted indanes B by the reaction of readily prepared 3-substituted indenes A with commercially available arylboronic acids by using various TEMPO derivatives as external oxidants and Pd(OAc)2 as a catalyst. The anti,anti isomers are formed and reactions occur stereospecifically under mild conditions.
Fröhlich, Roland | Organisch-Chemisches Institut |
Kirchberg, Sylvia | Organisch-Chemisches Institut |
Studer, Armido | Professur für Organische Chemie (Prof. Studer) |