13407-35-7Relevant academic research and scientific papers
Stereospecific double glycolisation of 1,2-dihydropyridines with OsO4. Synthesis of (±) aminoarabinose- and of (±) aminoaltrose derivatives [1]
Backenstrass, Frededrique,Streith, Jacques,Tschamber, Theophile
, p. 2139 - 2142 (1990)
Double glycolisation of 1,2-dihydropyridines 1 led stereospecifically and in good yield to the corresponding (±) aminoarabinose- and (±) aminoaltrose derivatives 5. Hydrogenolysis of the N-benzyloxy carbonyl piperidinose 5b gave directly the 1-desoxy derivative 7a.
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
