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. Author manuscript; available in PMC: 2011 Mar 20.
Published in final edited form as: Tetrahedron. 2010 Mar 20;66(12):2175–2180. doi: 10.1016/j.tet.2010.01.053

Table II.

Initial rates and enantioselectivities for the product formation in the transesterification reaction of different sec-alcohols with vinyl butyrate for subtilisin Carlsberg co-lyophilized with MβCD

Substrates VSa VRa Eb Substrates VSa VRa Eb
First Group Second Group
graphic file with name nihms-172780-t0011.jpg 177 59 3 graphic file with name nihms-172780-t0012.jpg 255 28 9
graphic file with name nihms-172780-t0013.jpg 246 12 20 graphic file with name nihms-172780-t0014.jpg 139 1.9 73
graphic file with name nihms-172780-t0015.jpg 102 2.3 44 graphic file with name nihms-172780-t0016.jpg 59 0.4 141
graphic file with name nihms-172780-t0017.jpg 99 1.7 58 graphic file with name nihms-172780-t0018.jpg 209 2.6 80
graphic file with name nihms-172780-t0019.jpg 183 2.7 67
Third Group Fourth Group
graphic file with name nihms-172780-t0020.jpg 139 1.9 73 graphic file with name nihms-172780-t0021.jpg 74 1.4 51
graphic file with name nihms-172780-t0022.jpg 228 2.2 104 graphic file with name nihms-172780-t0023.jpg 49 24.5 2
graphic file with name nihms-172780-t0024.jpg 14 0.1 126c
graphic file with name nihms-172780-t0025.jpg 32 0.1 240c
a

Initial rates for the S- and R-enantiomer in nmol mg−1min−1

b

Measured by the ratio of [kcat/KM]S/[kcat/KM]R = VS[R]/VR[S]

c

Enantioselectivity could not be determined accurately because of the very low value of VR