@article{wjoc2013124,
author={Elkanzi, N. A. A.},
title={Short Review on Synthesis of Thiazolidinone and ¦Â-Lactam},
journal={World Journal of Organic Chemistry},
volume={1},
number={2},
pages={24--51},
year={2013},
url={http://pubs.sciepub.com/wjoc/1/2/4},
abstract={The review summarizes literature dealing with the synthesis of thiazolidinoneand ¦Â-lactamVarious methods for synthesis of thiazolidinone and ¦Â-lactamare discussed. Like boiling benzene thioglycolic acid was added to (1)a-d using a water separator to give thiazolidinone derivatives (2)a-d. Also Reaction of the Schiff bases of 3 and /or5 with one mole of thioglycolic acid was proceeded smoothly to afford the corresponding thiazolidinone derivatives 6,7 respectively. The synthesis of a new type of compound, 2-hydrazolyl-5,5-diphenyl-4-thiazolidinone (24), obtained by treatment of thiosemicarbazone with benzyl in basic media. ¦Â-lactams were prepared by <i>N</i>-Tosyl-3-halo-3-butenylamines underwent efficient Ullmann-type coupling to afford 2-alkylideneazetidines, which could be readily converted to the corresponding ¦Â-lactams by oxidation with O<SUB>3 </SUB>to give ¦Â-lactams 119. A chiral N-heterocyclic carbene catalyzed the Staudinger reaction of arylalkylketenes with a variety of <i>N</i>-tert-butoxycarbonylarylimines to give the corresponding <i>cis</i>-¦Â-lactams 124.},
doi={10.12691/wjoc-1-2-4}
publisher={Science and Education Publishing}
}