Research Journal of Applied Sciences

Year: 2007
Volume: 2
Issue: 6
Page No. 759 - 762

Synthesis and Characterization Spectroscopic of the Chiral 1, 3-Oxazolidines

Authors : M. Dali , H. Boudiaf and A. Boukhari

Abstract: The condensation of para-substituted aromatic aldehydes with 1, 2-aminoalcohols such as (L)-prolinol, gives 1, 3- oxazolidines (potential proinsecticides). Starting of (S) amino alcohol, thanks to asymmetric carbone C2, we can obtain (S, S) and (S, R) diastereoisomers. The substituent situated on para position to aldehyde function in aromatic ring, affects the obtained proportion on diastereoisomers. If it is an electro-donor, the (S, S) diastereoisomer is clearly dominent; if it is an electro-attractor, the proportion of (S, S) and (S, R) diastereoisomers is practically the same.

How to cite this article:

M. Dali , H. Boudiaf and A. Boukhari , 2007. Synthesis and Characterization Spectroscopic of the Chiral 1, 3-Oxazolidines . Research Journal of Applied Sciences, 2: 759-762.

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