Journal of the Chemical Society. Chemical communications p. 161 - 163 (1986)
Update date:2022-07-30
Topics:
Bose, Ajay K.
Hegde, Vinod R.
Wagle, Dilip R.
Bari, Shamsher S.
Manhas, Maghar S.
3,4-Disubstituted-1-arylazetidin-2-ones can be prepared in an enantiospecific manner by the annelation of Schiff bases from optically active glyceraldehyde acetonide and their stereochemistry determined from n.m.r. studies on lactones prepared from these
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