Abstract
The use of the high pressure technique enables reduction of organic halides by tri-n-butyltin hydride to be carried out in the absence of a catalyst or free radical initiator. It leads to a better conservation of the structure of the starting material during the reduction. In the case of some unsaturated halides, a new chemoselectivity has been observed in favour of the addition of the hydride on the carboncarbon double bond.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have