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A synthesis of a new alkaloid-fullerene conjugate (1) is reported. The reaction was carried out by photoinduced [3+2] cycloaddition of the Alstonia indole alkaloid, 6,7- seco-angustilobine B (2), to fullerene[C 60 ] (3) under aerobic conditions. The major monoaddition photoadduct (1) was characterized unambiguously by UV, IR, MALDI-TOFMS and NMR experiments. A mechanism highlighted by sequential photoinduced electron transfer and radical recombination pathways is also proposed. No significant enhancement in inhibition against M. tuberculosis H 37 Rv was observed for 1 compared with its parent compounds 2 and 3.

Photoactivated [3+2] Addition of 6,7-seco-angustilobine B to Fullerene [C60]

Photoactivated [3+2] Addition of 6,7-seco-angustilobine B to Fullerene [C₆₀]