Journals

• Reekie, T., Banwell, M., Willis, A. (2012). A Raney-Cobalt-Mediated Tandem Reductive Cyclization Route to the 1,5-Methanoazocino[4,3‑b]indole Framework of the Uleine and Strychnos Alkaloids. The Journal of Organic Chemistry.
• Tan, S., Banwell, M., Willis, A., Reekie, T. (2012). Application of a Raney-Cobalt-Mediated Tandem Reductive Cyclization Protocol to Total Syntheses of the Aspidosperma Alkaloids (+-)-Limaspermidine and (+-)-1-Acetylaspidoalbidine. Organic Letters, 14(22), 5621-5623.
• Banwell, M., Jones, M., Reekie, T. (2011). The Palladium-Catalysed Ullmann Cross-Coupling Reaction. Chemistry in New Zealand, 75(3), 122-127.
• Austin, K., Matveenko, M., Reekie, T., Banwell, M. (2008). Chemoenzymatic methods for the ennatioselective assembly of bioactive natural products. Chemistry in Australia, 75(11), 3-7.
• Reekie, T., Austin, K., Banwell, M., Willis, A. (2008). The Chemoenzymatic Total Synthesis of Phellodonic Acid, a Biologically Active and Highly Functionalized Hirsutane Derivative Isolated from the Tasmanian Fungus Phellodon melaleucus. Australian Journal of Chemistry: an international journal for chemical science, 61(2), 94-106.

Conferences

• Reekie, T., Austin, K., Banwell, M. (2012). A Chemoenzymatic Total Synthesis of (-)- Phellodonic Acid. 28th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Sydney: RACI.
• Reekie, T., Banwell, M. (2012). A Concise Synthesis of the ABCDE Ring-system of Strychnine. 19th International Conference on Organic Synthesis, Melbourne: Arinex.
• Reekie, T., Banwell, M. (2011). A Cascade Approach to the Synthesis of the ABCDE Ring-system of Strychnine. Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Natural Products Group, Australia: Royal Australian Chemical Institute.
• Reekie, T., Banwell, M. (2011). A Synthesis of the ABCDE Ring-system of Strychnine. 23rd International Congress on Heterocyclic Chemistry, Scotland.
• Reekie, T., Banwell, M. (2010). A Synthesis of the ABCDE Ring-system of Strychnine. 31st Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.
• Reekie, T., Banwell, M. (2009). Strychnine Synthesis Support Studies: A Novel Approach to the ABCDE Ring-system. 30th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.
• Reekie, T., Austin, K., Banwell, M. (2008). A Chemoenzymatic Total Synthesis of (-)-Phellodonic Acid. 5th SINO-Australia Organic Chemistry Symposium, Australia: Australian National University (ANU).
• Reekie, T., Austin, K., Banwell, M. (2008). A Chemoenzymatic Total Synthesis of (-)-Phellodonic Acid. 29th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.
• Reekie, T., Banwell, M. (2008). The Enantioselective Construction of a Key Intermediate for the Synthesis of Biologically Active Sesquiterpenoids Incorporating Novel Ring Systems. 23rd Royal Australian Chemical Institute Organic Chemistry Conference, Australia: RACI.

2012

• Reekie, T., Austin, K., Banwell, M. (2012). A Chemoenzymatic Total Synthesis of (-)- Phellodonic Acid. 28th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Sydney: RACI.
• Reekie, T., Banwell, M. (2012). A Concise Synthesis of the ABCDE Ring-system of Strychnine. 19th International Conference on Organic Synthesis, Melbourne: Arinex.
• Reekie, T., Banwell, M., Willis, A. (2012). A Raney-Cobalt-Mediated Tandem Reductive Cyclization Route to the 1,5-Methanoazocino[4,3‑b]indole Framework of the Uleine and Strychnos Alkaloids. The Journal of Organic Chemistry.
• Tan, S., Banwell, M., Willis, A., Reekie, T. (2012). Application of a Raney-Cobalt-Mediated Tandem Reductive Cyclization Protocol to Total Syntheses of the Aspidosperma Alkaloids (+-)-Limaspermidine and (+-)-1-Acetylaspidoalbidine. Organic Letters, 14(22), 5621-5623.

2011

• Reekie, T., Banwell, M. (2011). A Cascade Approach to the Synthesis of the ABCDE Ring-system of Strychnine. Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Natural Products Group, Australia: Royal Australian Chemical Institute.
• Reekie, T., Banwell, M. (2011). A Synthesis of the ABCDE Ring-system of Strychnine. 23rd International Congress on Heterocyclic Chemistry, Scotland.
• Banwell, M., Jones, M., Reekie, T. (2011). The Palladium-Catalysed Ullmann Cross-Coupling Reaction. Chemistry in New Zealand, 75(3), 122-127.

2010

• Reekie, T., Banwell, M. (2010). A Synthesis of the ABCDE Ring-system of Strychnine. 31st Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.

2009

• Reekie, T., Banwell, M. (2009). Strychnine Synthesis Support Studies: A Novel Approach to the ABCDE Ring-system. 30th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.

2008

• Reekie, T., Austin, K., Banwell, M. (2008). A Chemoenzymatic Total Synthesis of (-)-Phellodonic Acid. 5th SINO-Australia Organic Chemistry Symposium, Australia: Australian National University (ANU).
• Reekie, T., Austin, K., Banwell, M. (2008). A Chemoenzymatic Total Synthesis of (-)-Phellodonic Acid. 29th Annual One-Day Symposium, Royal Australian Chemical Institute, NSW Organic Chemistry Group, Australia: Royal Australian Chemical Institute.
• Austin, K., Matveenko, M., Reekie, T., Banwell, M. (2008). Chemoenzymatic methods for the ennatioselective assembly of bioactive natural products. Chemistry in Australia, 75(11), 3-7.
• Reekie, T., Austin, K., Banwell, M., Willis, A. (2008). The Chemoenzymatic Total Synthesis of Phellodonic Acid, a Biologically Active and Highly Functionalized Hirsutane Derivative Isolated from the Tasmanian Fungus Phellodon melaleucus. Australian Journal of Chemistry: an international journal for chemical science, 61(2), 94-106.
• Reekie, T., Banwell, M. (2008). The Enantioselective Construction of a Key Intermediate for the Synthesis of Biologically Active Sesquiterpenoids Incorporating Novel Ring Systems. 23rd Royal Australian Chemical Institute Organic Chemistry Conference, Australia: RACI.