Abstract
The Lewis acid-catalyzed cyclocondensation of methylthio (or phenylthio)-silyloxydienes (2), easily derived from stable sulfur ylides (1), with several aromatic aldehydes (3) was investigated. Namely, in the case of boron trifluoride normal reaction products, 2, 3-dihydro-4-pyrones (4), were obtained in good yields. Novel reaction products, thiolanium ylides (6 and 7), were obtained in the presence of titanium(IV) chloride. The structures of 6g was established by X-ray crystallography.
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.
