Abstract
AbstractNew 3‐acylamino‐2‐oxazolidinone derivatives 3 were obtained in good yields by reaction of 5‐aryl (or benzyl)3‐(2‐hydroxyethyl)1,3,4‐oxadiazol‐2(3H)ones 1 with sodium ethylate. Treatment of ethyl 5‐aryl‐2‐oxo‐1,3,4‐oxadiazole‐3(2H)‐acetates 7 with aromatic aldehydes in the presence of sodium ethylate or sodium hydride afforded 3‐acylamino‐5‐aryl‐4‐ethoxycarbonyl‐2‐oxazolidinone derivatives as two trans‐5 and cis‐6 racemics. Only RS,SR‐racemates were obtained with acetophenone under the same conditions.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
