Date of Award
6-2000
Document Type
Open Access
Degree Name
Bachelor of Science
Department
Chemistry
Language
English
Abstract
A mild and versatile synthesis of a-oxy-6-amino esters has been performed by condensation of the chlorotitanium enolates of methyl methoxyacetate with aldimines. The imine-aldol addition occurs in excellent yields without Lewis acid activation of the imine. All aryl imines examined show good to excellent diastereoselection for the anti isomers.
Recommended Citation
Barkin, Julia Leigh, "Diastereoselection in titanium enolate addition to aldmines" (2000). Honors Theses. 2072.
https://digitalworks.union.edu/theses/2072
Rights Statement
