Abstract
Abstract Phenylcarbene generated in acetone solution gives oxirane, vinyl ether and 1,3-dioxolane presumably via initial attack of the singlet state on the lone pair electrons of carbonyl oxygen leading to a carbonyl ylide, whereas a C–H insertion product arising from the triplet markedly increases in matrix environments.
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.
