133696-29-4Relevant articles and documents
Diastereoselective hydroboration of chiral enamines using an enantiomerically pure amine from an industrial waste material as the source of chirality
Pennemann, Helmut,Wallbaum, Sabine,Martens, Juergen
, p. 2133 - 2142 (2007/10/03)
By a hydroboration/oxidation procedure trans-aminoalcohols with dr values from 74:26 to ≥95:5 were obtained. A bicyclic amine derived from the unnatural amino acid 2-azabicyclic[3.3.0]octane-3-carboxylic acid was used as the chiral precursor. The absolute