Switching from S- to R-Selectivity in the Candida antarctica Lipase B-Catalyzed Ring-Opening of ö-Methylated Lactones: Tuning Polymerizations by Ring Size
Switching from S- to R-Selectivity in the Candida antarctica Lipase B-Catalyzed Ring-Opening of ö-Methylated Lactones: Tuning Polymerizations by Ring Size
- J. Am. Chem. Soc., 129(23), p.7393-7398, 2007 .
Novozym 435-catalyzed ring-opening of a range of ö-methylated lactones demonstrates fascinating differences in rate of reaction and enantioselectivity. A switch from S- to R-selectivity was observed upon going from small (ring sizes e7)to large lactones (ring sizes g8). This was attributed to the transition from a cisoid to a transoid conformational preference of the ester bond on going from small to large lactones. The S-selectivity of the ring-opening of the small, cisoid lactones was low to moderate, while the R-selectivity of the ring-opening of the large transoid lactones was surprisingly high. The S-selectivity of the ring-opening of the small, cisoid lactones combined with the established R-selectivity of the transesterification of (aliphatic)secondary alcohols prevented polymerization from taking place. Ringopening of the large, transoid lactones wasR-selective with high enantioselectivity. As a result, these lactones could be polymerized, without exception, by straightforward kinetic resolution polymerization, yielding the enantiopure R-polyester with excellent enantiomeric excess (>99
Novozym 435-catalyzed ring-opening of a range of ö-methylated lactones demonstrates fascinating differences in rate of reaction and enantioselectivity. A switch from S- to R-selectivity was observed upon going from small (ring sizes e7)to large lactones (ring sizes g8). This was attributed to the transition from a cisoid to a transoid conformational preference of the ester bond on going from small to large lactones. The S-selectivity of the ring-opening of the small, cisoid lactones was low to moderate, while the R-selectivity of the ring-opening of the large transoid lactones was surprisingly high. The S-selectivity of the ring-opening of the small, cisoid lactones combined with the established R-selectivity of the transesterification of (aliphatic)secondary alcohols prevented polymerization from taking place. Ringopening of the large, transoid lactones wasR-selective with high enantioselectivity. As a result, these lactones could be polymerized, without exception, by straightforward kinetic resolution polymerization, yielding the enantiopure R-polyester with excellent enantiomeric excess (>99