The non-genotoxic carcinogens naphthalene and para-dichlorobenzene suppress apoptosis in C, Nature Chemical Biology, 2006 Synthesis of naturally occurring naphthoquinone epoxides and application in the synthesis of β-lapachone, Org. Biomol. Chem., 2010 Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine, Org. Biomol. Chem., 2010, 8, 3426. Synthesis of 1,2-annulated and 1,2-unsubstituted pyrrolo[2,1,5-de]quinolizin-5-ones (cycl[3.3.2]azin-5-ones) via [3+2] cycloadditions of 1-oxoquinolizinium ylides with cyclic alkenes, Org. Biomol. Chem., 2010, 8, 4921. A photosensing system composed of photosystem I, molecular wire, gold nanoparticle, and double surfactants in water, Chem. Commun., 2010, 46, 2557. An isolable o-quinodimethane and its fixation of molecular oxygen to give an endoperoxide, Chem. Commun., 2009, 4821. Characterization, reactivity and photosensitizing properties of the triplet excited state of α-lapachone, Phys. Chem. Chem. Phys., 2008, 10, 6645. The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyteglutathione reductase, Org. Biomol. Chem., 2008, 6, 2731. Surface photochemistry of the herbicidenapropamide. The role of the media and environmental factors in directing the fates of intermediates, Photochem. Photobiol. Sci., 2008, 7, 69.