. 2023 Dec 29;29(1):201. doi: 10.3390/molecules29010201

Table 8.

Most successful photochemical reactions of the starting compounds 1–5 were performed in a flow reactor (followed by HPLC *).

Comp.	Catalyst	Retention Time (min)	Wavelength (nm)/Temp. °C	Flow Rate (mL/min)	Conversion (%)	Productivity (μmol mL⁻¹ min⁻¹)	Yields of Photoproducts (%)
Comp.	Catalyst	Retention Time (min)	Wavelength (nm)/Temp. °C	Flow Rate (mL/min)	Conversion (%)	Productivity (μmol mL⁻¹ min⁻¹)	cis-	Dimer	Cycl. **	trans-	Undefined
1	-	2	365/22	0.5	94	0.470	94.0	-	-	6.0	-
2	-	2	365/22	0.5	61.6	0.308	61.6	-	-	38.4	-
3	-	2	365/22	0.5	91.7	0.458	71.0	-	-	8.3	20.7
4	-	2	365/22	0.5	92.2	0.461	81.9	-	-	7.8	10.3
5	-	2	365/22	0.5	91.0	0.455	22.5	4.8	29.8	9.0	30.1
1	FbA	10	420/22	0.1	100	0.500	-	58.1	19.3	-	22.6
2	FbA	10	420/22	0.1	40.2	0.201	8.1	-	-	59.8	32.1
3	FbA	10	420/22	0.1	100	0.500	-	6.4	93.6	-	-
4	FbA	10	420/22	0.1	100	0.500	-	58.0	13.8	-	28.1
5	FbA	10	420/22	0.1	100	0.500	-	-	90.1	-	9.9

HPLC analyses values read at 320 nm; ** product of photochemical electrocyclization reaction.