A One-Step Synthesis of Pseudoephedrine Glycinamide, a Versatile Precursor for the Synthesis of a-Amino Acids
Access StatusFull text of the requested work is not available in DASH at this time ("dark deposit"). For more information on dark deposits, see our FAQ.
Gleason, James L.
MetadataShow full item record
CitationMyers, Andrew G., Taeyoung Yoon, and James L. Gleason.
AbstractBoth enantiomers of a pseudoephedrine glycinamide [(+)- or (-)-1] were synthesized by either of two procedures: (1) a standard two-step coupling of N-Boc-Gly with pseudoephedrine followed by deprotection, or (2) a more economical one-step coupling reaction of Gly-OMe with pseudoephedrine mediated by LiCl and base.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:4725866
- FAS Scholarly Articles