Author:
Soliman SA,Abdine H,El-Nenaey S
Abstract
The synthesis of 15
diastereomeric oxazolidine derivatives of the type 2-(substituted phenyl)-3,4-dimethyl-5-phenyloxazolidine
is reported. The specific as well as the molecular rotations of 31
diastereomeric oxazolidine derivatives of the same type of structure were
determined. The cis com- pounds have higher specific and molecular rotation
than the corresponding trans isomers. Substitution in the ortho or para
position increased specific and molecular rotation while substitution in the
meta position had an opposite effect. ��� The infrared spectra of 26 oxazolidine
derivatives, having either a cis or a trans type of configuration, have been
recorded in the range 2000-700 cm-1.
Cited by
25 articles.
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