e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Tetrahedron letters
Diastereoselektive Synthese von α, γ-aminoalkoholen durch intramolekulare 1, 3-dipolare Cycloaddition von Nitronen mit Allylthioether-Gruppierung und …
HG Aurich, KD Möbus
Index: Aurich, Hans Guenter; Moebus, Klaus-Dieter Tetrahedron Letters, 1988 , vol. 29, # 45 p. 5755 - 5758
Abstract The bicyclic compounds 2 and 4 are formed by intramolecular 1, 3-dipolar cycloaddition of the nitrones 1 and 3, respectively. Reductive cleavage of 2a and 4a with desulfurization yields α, γ-aminoalcohols 7 and 9, respectively, as diastereomerically pure compounds.
