1,2,3-Trisubstituted Indanes by Highly Diastereoselective Palladium-Catalyzed Oxyarylation of Indenes with Arylboronic Acids and Nitroxides

Kirchberg S, Frohlich R, Studer A

Forschungsartikel (Zeitschrift)

Zusammenfassung

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.

Details zur Publikation

FachzeitschriftAngewandte Chemie International Edition (Angew. Chem. Int. Ed.)
Jahrgang / Bandnr. / Volume49
Ausgabe / Heftnr. / Issue38
Seitenbereich6877-6880
StatusVeröffentlicht
Veröffentlichungsjahr2010 (31.12.2010)
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1002/anie.201002214
Stichwörterhomogeneous catalysis nitroxides palladium stereoselective reactions synthetic methods c-h arylation grignard-reagents organic-synthesis bond formation alkenes tempo inhibitors carboamination diamination aryl

Autor*innen der Universität Münster

Fröhlich, Roland
Organisch-Chemisches Institut
Kirchberg, Sylvia
Organisch-Chemisches Institut
Studer, Armido
Professur für Organische Chemie (Prof. Studer)