Publication
A total asymmetric synthesis of the polyol subunit of the polyene macrolide antibiotic RK-397 was developed through the stereoselective functionalization of (1R,1’S,6S,6’R)-3,3’-methylenebis(cyclohept-3-ene-1,6-diol). The pathway generates a large variety of stereoisomeric intermediates and thus can be applied to the preparation of analogues of the natural antibiotic.
César Pulgarin, Stefanos Giannakis, Truong-Thien Melvin Le, Jérémie Decker
Ivo Furno, Alan Howling, Fabio Avino, Rita Agus, Brayden Graham Myers, Lorenzo Ibba, Leonardo Zampieri
Sandor Kasas, María Inés Villalba