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. 2018 Sep 12;57(41):13648–13651. doi: 10.1002/anie.201807119

Table 1.

Substrate scope of the photoenzymatic decarboxylation reaction.[a] Inline graphic

Substrate [Product] [mm] Conversion [%][b] TON (CvFAP)[c]
C12H24O2
(lauric acid)
3.0 11 500
C14H28O2
(myristic acid)
6.9 25 1150
C16H32O2
(palmitic acid)
27.7 96 4610
C17H34O2
(margaric acid)
28.7 96 4780
C18H36O2
(stearic acid)
26.1 92 4350
C18H34O2 (Δ9)
(oleic acid)
17.7 65[d] 2950
C18H32O2 (Δ9, 12)
(linoleic acid)
14.6[c] 49[d] 2600
C20H40O2
(arachidic acid)
25.7 90 4580

[a] Reaction conditions: [substrate]=30 mm, [CvFAP]=6.0 μm, Tris‐HCl buffer (pH 8.5, 100 mm), 30 % DMSO, illumination with blue light (intensity=13.7 μE L−1 s−1) for 14 h. [b] Conversion: [product]final×([product]final+[substrate]final)−1. [c] TON: [product]final×[CvFAP]−1. [d] Due to the lack of a standard reference, the conversion was calculated by using: conversion=([substrate]initial− [substrate]final)×[substrate]initial −1.