Abstract
The reaction of 5-oxotetrahydro-4H-thiochromenes with Grignard reagents has been studied and it has been shown that the reagent adds to the 1,2-position of the conjugated system in the cyclic ketones, The structure of the products depends on that of the starting cyclic ketone.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have