25531-85-5Relevant academic research and scientific papers
De novo synthesis of racemic altronolactam and arabinonolactam azasugars
Tschamber, Theophile,Rodriguez-Perez, Elsa-Maria,Wolf, Patrick,Streith, Jacques
, p. 669 - 676 (2007/10/03)
Starting from the known peracetylated piperidinose derivatives (7a) and (7b), the corresponding altrono- and arabinono-lactams (4) and (5) were obtained in a straightforward way. A selective two-step hydrolysis of the anomeric acetoxy groups gave the free
Stereoselective catalytic double osmylation of 1,2-dihydropyridines leading to amino-arabinose and to amino-altrose derivatives and to potential glycosidase inhibitors
Tschamber, Theophile,Backenstrass, Frederique,Neuburger, Marcus,Zehnder, Margareta,Strieth, Jacques
, p. 1135 - 1152 (2007/10/02)
Catalytic double osmylation of 1,2-dihydropyridines 1b and 1c proceeded stereospecifically and in good yields to the corresponding aminoarabinose 2b, and aminoaltrose 2c derivatives, respectively. In basic medium these piperidinoses equilibrated with thei
