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. 2013 Oct 16;18(10):12820–12844. doi: 10.3390/molecules181012820

Table 1.

Synthesis of cyclovertrylenes a.

Entry Alcohol Products Yield% b
MW c IR d
1 graphic file with name molecules-18-12820-i009.jpg graphic file with name molecules-18-12820-i010.jpg 85 80
graphic file with name molecules-18-12820-i011.jpg 1 3
graphic file with name molecules-18-12820-i012.jpg 2 5
graphic file with name molecules-18-12820-i013.jpg 4 5
graphic file with name molecules-18-12820-i014.jpg 8 7
2 graphic file with name molecules-18-12820-i015.jpg graphic file with name molecules-18-12820-i016.jpg 90 88
graphic file with name molecules-18-12820-i017.jpg 10 12
3 graphic file with name molecules-18-12820-i018.jpg graphic file with name molecules-18-12820-i019.jpg 80 75
graphic file with name molecules-18-12820-i020.jpg 5 5
graphic file with name molecules-18-12820-i021.jpg 15 20

a Reaction conditions: benzyl alcohols 1a3a (2 mmol) and TAFF (20 mg); b Yield of isolated product after chromatographic purification; c Microwave at 85 °C (100W), 1.50–5 min; d IR at 95 °C (375W), 3–7 min.