128013-88-7Relevant academic research and scientific papers
Hydride reagents for stereoselective reductive amination. An improved preparation of 3-endo-tropanamine
McGill, John M.,Labell, Elizabeth S.,Williams, MaryAnn
, p. 3977 - 3980 (2007/10/03)
The reductive amination of substituted cyclohexanones with sodium triacyloxyborohydrides derived from NaBH4 and various carboxylic acids provides highly diastereoselective conversions to protected axial amines. This method was applied to the stereoselective preparation of 3-endo-tropanamine.
