2024/05/08 by Felix Flachsmann, Natalie Aeberli, Sandro Dossenbach +8 · 1 voice
Biochemistry, Genetics and Molecular Biology · #Enzyme Catalysis and Immobilization #Microbial Metabolic Engineering and Bioproduction #Biochemical Acid Research Studies
paper · doi:10.1002/hlca.202400016
Abstract All eight theoretical stereoisomers of (10 S )‐Ambrox have been synthesized by enzymatic polycyclization of the four geometric isomers of homofarnesol with selected squalene hopene cyclases. This includes the highly strained (+)‐(8 S ,9 S)‐ Ambrox, an isomer historically considered unlikely to exist. The enantiomeric (10 R )‐series has been prepared by a combination of diastereoselective synthesis and preparative chiral HPLC. Thus, for the first time, the synthesis and sensory properties of all but one stereoisomers of Ambrox are presented. The results solve a long standing peradventure: the commercial product (−)‐Ambrox exhibits by far the strongest odour, the previously described 9‐ epi ‐Ambrox is 26 times weaker. The enantiomer difference between (−)‐and (+)‐Ambrox was also found much higher than in previous reports (1000 vs. 8 times). The (8 R )‐configuration was identified as the single most important structural feature for high odour strength.