93474-90-9Relevant academic research and scientific papers
Enantioselective synthesis of oxazolidinones from N,N-dibenzylamino epoxides
Vargas, Gabriel E.,Afonso, María M.,Palenzuela, J. Antonio
experimental part, p. 1471 - 1473 (2009/10/17)
Enantiomerically pure oxazolidinones are easily prepared from N,N-dibenzylamino epoxides through a one-pot procedure involving monodeprotection of the amino group and treatment with NaHCO3. Georg Thieme Verlag Stuttgart.
Synthesis of Protected Aminocyclohexanediols
Knapp, Spencer,Patel, Dinesh V.
, p. 5072 - 5076 (2007/10/02)
As the model study for the synthesis of aminocyclitols and amino sugars, 2-cyclohexen-1-ol (1) was converted to five of the seven possible (1,2,3)-aminocyclohexanediols in protected form (4a, 6a, 11a, 13a, and 18a).Two flexible new approaches were employe
