STEREOCONTROLLED SYNTHESIS OF (9<i>S</i>)-KETODECANOLIDE ON THE BASIS OF MICHAEL ADDUCTS OBTAINED FROM LEVOGLUCOSENONE AND CYCLOHEXANONE
DOI:
https://doi.org/10.1007/4553Keywords:
ketodecanolide, lactones, levoglucosenone, Michael adducts, ketalizationAbstract
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