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. 2016 Apr 20;21(4):517. doi: 10.3390/molecules21040517

Table 1.

Chemically synthesized CoA-thioesters. Products were confirmed by HPLC-MS. Yield was determined with HPLC-UV at 260 nm.

Acyl-CoA Yield (%) Used Method 1
Acetyl-CoA 1 81 anhydride
Propionyl-CoA 2 86 anhydride
Butyryl-CoA 3 87 anhydride
Hexanoyl-CoA 4 76 CDI
Heptanoyl-CoA 5 74 CDI
Octanoyl-CoA 6 68 CDI
Lauryl-CoA 7 67 CDI
Acrylyl-CoA 8 17 ECF
3,3-Dimethylacrylyl-CoA 9 39 ECF
Crotonyl-CoA 10 80 anhydride
Octenoyl-CoA 11 57 ECF
Sorbityl-CoA 12 61 ECF
Cinnamoyl-CoA 13 75 ECF
Isobutyryl-CoA 14 68 CDI
2-Methylbutyryl-CoA 15 78 CDI
3-Hydroxypropionyl-CoA 16 66 CDI
3-(R)-Hydroxybutyryl-CoA 17 54 CDI
3-(S)-Hydroxybutyryl-CoA 18 57 CDI
6-Oxoheptanoyl-CoA 19 56 CDI
Succinyl-CoA 20 86 anhydride
Methylsuccinyl-CoA 21 40 CDI

1 If multiple synthesis methods were successful only the one with the highest yield is listed (see also Table S1).