Abstract
Abstract The reaction of 1-phenylselenocyclopropylmethanols with TsOH in methanol proceeded smoothly to afford the homoallylic ethers, ring-enlargement products, and ring-opening products depending upon the kind of substituent on the cyclopropane ring or α-carbon. On the other hand, in the case of the absence of methanol as nucleophile, 4H-selenochromene derivatives were obtained exclusively.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
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 call
