Abstract
Under solar light at room temperature, the tungsten pentacarbonyl complex of the P–S–P-linked biphosphole (6) undergoes a [2+2] intramolecular cycloaddition. Then, this [2+2] dimer (7) gives the original [4+4] dimer (8) via a Cope rearrangement. This sequence stands in sharp contrast with the behavior of the corresponding P–O–P-linked biphosphole (2) which undergoes a classical [4+2] cycloaddition.
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.
