Abstract
The 1,3 dipolar cycloadditions of diazomethane and ethyl diazoacetate with differently substituted 5-sulfur-2(5 H)-furanones ( 1–6) are reported. Cycloaddition of diazomethane occurs in a regio- and stereospecific manner to give the expected adducts 9–14, in good yield. The cycloaddition with ethyl diazoacetate occurs also in a regio- and stereospecific manner, but affords the corresponding 2-pyrazolines 15–19.
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.
