Em P Nick Greeves MA PhD NTF SFHEA
Emeritus Professor Chemistry
- Work email Ngreeves@liverpool.ac.uk
- Personal Website3D interactive animations
- About
- Research
- Publications
- Teaching
- Professional Activities
Publications
Selected Publications
- Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide) (Journal article - 2014)
- Supporting lifelong learning: enhancing the value of interactive 3D chemistry (Report - 2010)
- Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts (Journal article - 2016)
- ChemTube3D for iOS (Software / Code - 2017)
- ChemTube3D 2019 responsive version for mobile (Software / Code - 2019)
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2021
360° Lab Safety exercises (Internet publication)
Gaynor, J., & Greeves, N. (2021). 360° Lab Safety exercises. Retrieved from https://www.chemtube3d.com/chemistry-health-and-safety-360-exercises/ChemTube3D: Health and Safety section (Other)
Gaynor, J., & Greeves, N. (2021). ChemTube3D: Health and Safety section. Retrieved from https://www.chemtube3d.com/category/360/2020
OBITUARY Stuart Warren (24 Dec 1938-22 Mar 2020) (Journal article)
Aggarwal, V. K., Armstrong, S. K., Caggiano, L., Chibale, K., Clayden, J., Coldham, I., . . . Wyatt, P. (2020). OBITUARY Stuart Warren (24 Dec 1938-22 Mar 2020). ORGANIC & BIOMOLECULAR CHEMISTRY, 18(37), 7236-7237. doi:10.1039/d0ob90121k2019
ChemTube3D 2019 responsive version for mobile (Software / Code)
Greeves, N. (2019). ChemTube3D 2019 responsive version for mobile (Version 3.0) [Computer Software]. Retrieved from https://www.chemtube3d.com/2018
Recent progress in the synthesis and applications of glycerol carbonate (Journal article)
Christy, S., Noschese, A., Lomeli-Rodriguez, M., Greeves, N., & Lopez-Sanchez, J. A. (2018). Recent progress in the synthesis and applications of glycerol carbonate. CURRENT OPINION IN GREEN AND SUSTAINABLE CHEMISTRY, 14, 99-107. doi:10.1016/j.cogsc.2018.09.003ChemTube3D for Android (Software / Code)
Greeves, N. (2018). ChemTube3D for Android (Version 1.0) [Computer Software]. Retrieved from https://play.google.com/store/apps/details?id=www.chemtube3d.com2017
ChemTube3D for iOS (Software / Code)
Greeves, N. (2017). ChemTube3D for iOS (Version 1.0.1) [Computer Software]. Retrieved from https://itunes.apple.com/gb/app/chemtube3d/id12919521622016
Back Cover: Visible‐Light‐Controlled Oxidation of Glucose using Titania‐Supported Silver Photocatalysts (ChemCatChem 22/2016) (Journal article)
Da Vià, L., Recchi, C., Davies, T. E., Greeves, N., & Lopez‐Sanchez, J. A. (2016). Back Cover: Visible‐Light‐Controlled Oxidation of Glucose using Titania‐Supported Silver Photocatalysts (ChemCatChem 22/2016). ChemCatChem, 8(22), 3556. doi:10.1002/cctc.201601429Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts (Journal article)
Da Via, L., Recchi, C., Davies, T. E., Greeves, N., & Lopez-Sanchez, J. A. (2016). Visible-Light-Controlled Oxidation of Glucose using Titania-Supported Silver Photocatalysts. CHEMCATCHEM, 8(22), 3475-3483. doi:10.1002/cctc.2016007752015
One-pot visible-light mediated photocatalytic hydrolysis and oxidation of cellobiose to gluconic acid and lower chain carbohydrates (Conference Paper)
Da Via, L., Davies, T., Greeves, N., & Lopez-Sanchez, J. (2015). One-pot visible-light mediated photocatalytic hydrolysis and oxidation of cellobiose to gluconic acid and lower chain carbohydrates. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 250. Retrieved from https://www.webofscience.com/2014
Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide) (Journal article)
Aspinall, H., Bacsa, J., Beckingham, O., Eden, E. G. B., Greeves, N., Hobbs, M. D., . . . Thomas, C. D. (2014). Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide). Dalton Transactions, 43(3), 1434-1442. doi:10.1039/C3DT52366G2011
A general and convenient route to oxazolyl ligands (Journal article)
Aspinall, H. C., Beckingham, O., Farrar, M. D., Greeves, N., & Thomas, C. D. (2011). A general and convenient route to oxazolyl ligands. TETRAHEDRON LETTERS, 52(40), 5120-5123. doi:10.1016/j.tetlet.2011.07.070Unusual Hybrid Materials Prepared by the Oxidation of a Ketone (Journal article)
Holden, D. L., Goulding, H. V., Bacsa, J., Berry, N. G., Greeves, N., Stephenson, R. A., . . . Fogg, A. M. (2011). Unusual Hybrid Materials Prepared by the Oxidation of a Ketone. CRYSTAL GROWTH & DESIGN, 11(7), 3013-3019. doi:10.1021/cg200286tChemPreLab (Journal article)
Sedghi, G., Berry, N., & Greeves, N. (2011). ChemPreLab. Wavelength, 7(1), 42-43.ChemPreLab: Chemistry pre-lab virtual experiments (Conference Paper)
Sedghi, G., Berry, N., Greeves, N., & Barnes, K. (2011). ChemPreLab: Chemistry pre-lab virtual experiments. In Variety Conference. York.Providing Recordings of Chemistry Teaching (Journal article)
Berry, N., Greeves, N., Aspinall, H., Bunyan, N., Barnes, K., Bradford, M., & Chin, P. (2011). Providing Recordings of Chemistry Teaching. Wavelength, 7(1), 6-9.2010
A new Yb<SUP>3+</SUP>-catalyzed pinacol and imine-coupling reaction (Journal article)
Aspinall, H. C., Greeves, N., & Hin, S. L. F. (2010). A new Yb<SUP>3+</SUP>-catalyzed pinacol and imine-coupling reaction. TETRAHEDRON LETTERS, 51(12), 1558-1561. doi:10.1016/j.tetlet.2010.01.057ChemTube3D Interactive 3D Organic Reaction Mechanisms (Software / Code)
Greeves, N., & Berry, N. G. (2010). ChemTube3D Interactive 3D Organic Reaction Mechanisms (Version 2.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/Supporting lifelong learning: enhancing the value of interactive 3D chemistry (Report)
Barnes, K., Greeves, N., Berry, N., Bunyan, N., & Strivens, J. (2010). Supporting lifelong learning: enhancing the value of interactive 3D chemistry. Bristol: JISC. Retrieved from http://www.jisc.ac.uk/whatwedo/programmes/elearning/ltig/ichem3d.aspx2009
ChemTube3D - Polymers (Software / Code)
Greeves, N., & Vernon, L. M. (2009). ChemTube3D - Polymers (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/polymerWorking with the Physical Sciences Centre (Journal article)
Greeves, N. (2009). Working with the Physical Sciences Centre. Wavelength, 5(2), 4-5.2008
ChemTube3D - Interactive 3D Solid State Structures (Software / Code)
Greeves, N., & Ho, S. K. (2008). ChemTube3D - Interactive 3D Solid State Structures (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/solidstateChemTube3D Interactive 3D Organic Reaction Mechanisms (Software / Code)
Greeves, N., Lawrenson, A., & Barnes, K. (2008). ChemTube3D Interactive 3D Organic Reaction Mechanisms (Version 1.0) [Internet (free access)]. Liverpool. Retrieved from http://www.chemtube3d.com/2005
(Journal article)
doi:10.1021/om050197Lanthanide pybox complexes as catalysts for enantioselective silylcyanation of aldehydes (Journal article)
Aspinall, H. C., Bickley, J. F., Greeves, N., Kelly, R. V., & Smith, P. M. (2005). Lanthanide pybox complexes as catalysts for enantioselective silylcyanation of aldehydes. ORGANOMETALLICS, 24(14), 3458-3467. doi:10.1021/om050197+Samarium diiodide-catalyzed diastereoselective pinacol couplings (Journal article)
Aspinall, H. C., Greeves, N., & Valla, C. (2005). Samarium diiodide-catalyzed diastereoselective pinacol couplings. ORGANIC LETTERS, 7(10), 1919-1922. doi:10.1021/ol050256f2003
Modular chiral polyether podands and their lanthanide complexes (Journal article)
Aspinall, H. C., Greeves, N., & McIver, E. G. (2003). Modular chiral polyether podands and their lanthanide complexes. TETRAHEDRON, 59(52), 10453-10463. doi:10.1016/j.tet.2003.06.008Short synthesis of a tetrasubstituted tetrahydropyran with five stereogenic centres-stereoselective double tandem rearrangements and cyclisation (Journal article)
Greeves, N., Lee, W. M., McLachlan, S. P., Oakes, G. H., Purdie, M., & Bickley, J. F. (2003). Short synthesis of a tetrasubstituted tetrahydropyran with five stereogenic centres-stereoselective double tandem rearrangements and cyclisation. TETRAHEDRON LETTERS, 44(50), 9035-9038. doi:10.1016/j.tetlet.2003.09.2092002
Defining effective chiral binding sites at lanthanides - highly enantioselective reagents and catalysts from binaphtholate and pybox ligands (Journal article)
Aspinall, H. C., & Greeves, N. (2002). Defining effective chiral binding sites at lanthanides - highly enantioselective reagents and catalysts from binaphtholate and pybox ligands. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 647(1-2), 151-157. doi:10.1016/S0022-328X(01)01370-5Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid (Journal article)
Aspinall, H. C., Bissett, J. S., Greeves, N., & Levin, D. (2002). Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid. TETRAHEDRON LETTERS, 43(2), 319-321. doi:10.1016/S0040-4039(01)02115-3Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid (Journal article)
Aspinall, H. C., Bissett, J. S., Greeves, N., & Levin, D. (2002). Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid. TETRAHEDRON LETTERS, 43(2), 323-325. doi:10.1016/S0040-4039(01)02116-52001
Chemistry in Britain review [6] (Journal article)
Greeves, N. (2001). Chemistry in Britain review [6]. Chemistry in Britain, 37(9), 25.2000
Pinwheel-shaped heterobimetallic lanthanide alkali metal binaphtholates: Ionic size matters! (Journal article)
Aspinall, H. C., Bickley, J. F., Dwyer, J. L. M., Greeves, N., Kelly, R. V., & Steiner, A. (2000). Pinwheel-shaped heterobimetallic lanthanide alkali metal binaphtholates: Ionic size matters!. ORGANOMETALLICS, 19(25), 5416-5423. doi:10.1021/om0006256Lithium binaphtholates: Chiral chains and clusters (Journal article)
Aspinall, H. C., Bickley, J. F., Dwyer, J. L. M., Greeves, N., & Steiner, A. (2000). Lithium binaphtholates: Chiral chains and clusters. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 39(16), 2858-2861. doi:3.0.CO;2-T">10.1002/1521-3773(20000818)39:16<2858::AID-ANIE2858>3.0.CO;2-TDOI: 10.1002/1521-3773(20000818)39:16<2858::AID-ANIE2858>3.0.CO;2-T