Abstract

An efficient route using nitroalkane synthon 3a and 3b for the synthesis of optically pure R-(+)-trans whisky lactone, (+)- 9 and R-(+)-eldanolide, (+)- 10 is described. In a key step, bakers' yeast reduction is employed to get the required chirality.

Full Text
Published version (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