Abstract
Abstract Treatment of Baylis–Hillman adducts with Et3SiH/I2 in CHCl3 at room temperature afforded the (Z)- and (E)-allyl iodides in stereoselective manner. The products are formed in excellent yields within 5 min. The method has successfully been utilized for synthesis of natural bioactive fatty acid amide, semiplenamide D.
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
