I. The stereochemistry of the opening of the imine ring with various reagents. II. The attempted reduction of naturally occuring threonine to 3-amino-2-butanol

I. The stereochemistry of the opening of the imine ring with various reagents. II. The attempted reduction of naturally occuring threonine to 3-amino-2-butanol

The 2,3-iminobutanes react with acetic acid to give products that are easily converted without isolation into 3-acetamido-2-acetoxybutanes. Comparisons of the latter with samples of known configuration demonstrate that ring opening occurs in a trans manner. Attempts to prepare 3-p-toluenesulfonamid...

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Bibliographic Details
Main Author: Ghirardelli, Robert George
Format: Others
Published: 1956
Online Access:https://thesis.library.caltech.edu/1061/1/Ghirardelli_rg_1956.pdf
Ghirardelli, Robert George (1956) I. The stereochemistry of the opening of the imine ring with various reagents. II. The attempted reduction of naturally occuring threonine to 3-amino-2-butanol. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/AF4V-BN43. https://resolver.caltech.edu/CaltechETD:etd-03232004-104542 <https://resolver.caltech.edu/CaltechETD:etd-03232004-104542>

Internet

https://thesis.library.caltech.edu/1061/1/Ghirardelli_rg_1956.pdf
Ghirardelli, Robert George (1956) I. The stereochemistry of the opening of the imine ring with various reagents. II. The attempted reduction of naturally occuring threonine to 3-amino-2-butanol. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/AF4V-BN43. https://resolver.caltech.edu/CaltechETD:etd-03232004-104542 <https://resolver.caltech.edu/CaltechETD:etd-03232004-104542>

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