89395-27-7Relevant academic research and scientific papers
SYNTHESIS OF A VERSATILE CHIRAL SYNTHON CORRESPONDING TO THE C(1) to C(7) SEGMENT OF 14-MEMBERED MACROLIDE ANTIBIOTICS
Born, Marco,Tamm, Christoph
, p. 2083 - 2086 (1989)
The synthesis of the C(1) to C(7) segment of a number of 14-membered macrolide antibiotics is described, starting from dimethyl 3-hydroxy-2,4-dimethylglutarate.
Stereoselective synthesis of a building block corresponding to the C(1)-to-C(7) moiety of 14-membered macrolide antibiotics
Born,Tamm
, p. 435 - 438 (2007/10/02)
The synthesis of 2',6'-dimethylphenyl (2R,3R,4R,5R,6S)-3-hydroxy-5,7-isopropylidenedioxy-2,4,6-trimethylhepta noate (13) a synthon for the C(1)-to-C(7) segment of a number of 14-membered macrolide antibiotics is described, starting from the meso-diester 3
