Abstract
AbstractThe effect of temp., solvent, and type of aldehyde on the stereospecific or stereoselective formation of azomethine ylides by the decarboxylative condensation of aldehydes with three types of α‐amino acids (a.a.'s): 1) cyclic sec. a.a.'s, 2) cyclic sec. a.a's with a benzylic carboxy group, and 3) acyclic prim. a.a.'s, is studied.
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