STEREOCONTROLLED SYNTHESIS OF (9S)-KETODECANOLIDE ON THE BASIS OF MICHAEL ADDUCTS OBTAINED FROM LEVOGLUCOSENONE AND CYCLOHEXANONE

Abstract

A synthetic route was developed consisting of 10 steps for the synthesis of ketodecanolide with native topology in 11% overall yield, starting from Michael adducts of levoglucosenone and cyclohexanone.

Authors: Liliya Kh. Faizullina*, Yuliya A. Khalilova, Shamil M. Salikhov, Farid A. Valeev