Abstract
AbstractThe recently described reaction between lithium hydride and addition products of acyl isothio‐cyanates with amines, methanol, and methanethiol in DMF followed by alkylation with methyl iodide is shown not to generate a new class of heterocycles – 2,2,4‐trisubstituted 2H‐1,3‐oxazetes – but to yield N‐acyl isothioureas, N‐acyl mono‐, and ‐dithioisocarbamates, respectively. The structures are confirmed by IR, mass, 1H‐NMR, and 13C‐NMR spectra.
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.
