Abstract
New 5-nitroimidazoles bearing a tetrasubstituted ethylenic double bond in 2-position were synthesized in high yields by the reaction of secondary nitronate anions with a new reductive alkylating agent, 1-methyl-2-trichloromethyl-5-nitroimidazole. Consecutive SRN1 and ERC1 mechanisms were followed in these processes.
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.
