(E)-4-[2-(bis(octadecylsulfanyl)tetrathiafulvalenyl)ethenyl]-1-methylpyridinium iodide: synthesis and characterisation of its Langmuir-Blodgett films

Andreu, R., Garin, J., Orduna, J., Ashwell, G. J., Amiri, M. A. & Hamilton, R., 3 Ebr 2002, Yn: Thin Solid Films. 407, 1-2, t. 236-239

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1,1,2 Tribromocyclopropanecarboxylic Acid and Derivatives Valuable Intermediates for Four Carbon Cyclopropane and Cyclopropene Synthons

Al-Dulayymi, A., Al-Dulayymi, J., Baird, M., Gerrard, M. E., Koza, G., Harkins, S. & Roberts, E., 1996, Yn: Tetrahedron. 52, t. 3409

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1,1′,2,2′-Tetralithioferrocene and 1,1′,2,2′,3,3′-Hexalithioferrocene: Useful Additions to Ferrocene Precursor Compounds

Butler, I., Evans, D., Horton, P., Coles, S. & Murphy, P., 8 Maw 2021, Yn: Organometallics. 40, 5, t. 600-605 6 t.

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100 years of anthropogenic impact causes changes in freshwater functional biodiversity

Eastwood, N., Zhou, J., Derelle, R., Abdallah, M.A.-E., Stubbings, W. A., Jia, Y., Crawford, S. E., Davidson, T. A., Colbourne, J. K., Creer, S., Bik, H., Hollert, H. & Orsini, L., 7 Tach 2023, Yn: Elife. 12

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2 Synthetic methods. Part (iii) Heteroatom methods

Murphy, P. J. & Thomas, D. A., 2000, Yn: Annual Reports on the Progress of Chemistry - Section B. 2000, 96, t. 39-63 25 t.

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2 Synthetic methods: Part (iv) Heteroatom methods

Murphy, P. J., 1998, Yn: Annual Reports on the Progress of Chemistry - Section B. 94, t. 51-75 25 t.

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2 Vinyl 1 1,1,2 trihalocyclopropanes Valuable Five Carbon Cyclopropane and Cyclopropene Synthetic Intermediates

Al-Dulayymi, A., Al-Dulayymi, J. & Baird, M., 1996, Yn: Tetrahedron. 52, 33, t. 10955

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2-Ethyl 5-methyl 3-hydroxythiophene-2,5-dicarboxylate.

Coles, S. J., Guthmann, H., Hursthouse, M. B. & Murphy, P. J., 1 Hyd 2001, Yn: Acta Crystallographica Section E: Structure Reports Online. 57, 10, t. o976-o977

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2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans

Wilson, R., Ainscough, R., Anderson, K., Baynes, C., Berks, M., Bonfield, J., Burton, J., Connell, M., Copsey, T., Cooper, J., Coulson, A., Craxton, M., Dear, S., Du, Z., Durbin, R., Favello, A., Fraser, A., Fulton , L., Gardner, A., Green, P., Hawkins, T., Hillier, L., Jier, M., Johnston, L., Jones, M., Kershaw, J., Kirsten, J., Laisstert, N., Latreille, P., Lightning, J., Lloyd, C., Mortimore, B., O'Callaghan, M., Parsons, J., Percy , C., Rifken, L., Roopra, A., Saunders, D., Shownkeen, R., Sims, M., Smaldon, N., Smith, A., Smith, M., Sonnhammer, E., Staden, R., Sulston, J., Thierry-Mieg, J., Thomas, K., Vaudin, M., Vaughan, K., Waterston, R., Watson, A., Weinstock, L., Wilkinson-Sproatt, J. & Wohldman, P., 3 Maw 1994, Yn: Nature. 368, 6466, t. 32-8 7 t.

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3,4-Phenylenedioxythiophenes (PheDOTs) functionalized with electron-withdrawing groupsand their analogs for organic electronics. Remarkably efficient tuning the energy levels in flatconjugated polymers

Krompiec, M. P., Baxter, S., Klimareva, E. L., Yufit, D. S., Congrave, D. G., Britten, T. K. & Perepichka, I., 14 Ebr 2018, Yn: Journal of Materials Chemistry C. 6, 14, t. 3746-3756

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