Resources

• Assaf, G.; Checksfield, G.; Critcher, D.; Dunn, P. J.; Field, S.; Harris, L. J.; Howard, R. M.; Scotney, G.; Scott, A.; Mathew, S.; Walker, G. M. H.; Wilder, A. The Use of Environmental Metrics to Evaluate Green Chemistry Improvements to the Synthesis of (s,s)-Reboxetine Succinate. https://pubs.rsc.org/en/content/articlelanding/2012/gc/c1gc15921f (accessed 2025-04-30).

  Dhangar, G.; Serrano, J. L.; Schulzke, C.; Gunturu, K. C.; Kapdi, A. R. Palladacycle-Catalyzed Triple Suzuki Coupling Strategy for the Synthesis of Anthracene-Based OLED Emitters. ACS Omega 2017, 2 (7), 3144–3156. https://doi.org/10.1021/acsomega.7b00725.

  Haidle, A.; Kohrt, J.; Liu, F. The Stille Reaction. https://hwpi.harvard.edu/files/myers/files/11-the_stille_reaction.pdf (accessed 2025-04-30).

  Heck, R. F. Palladium-Catalyzed Reactions of Organic Halides with Olefins. J. Org. Chem. 1982, 47 (15), 3223–3227. https://doi.org/10.1021/jo00096a072.

  Libretexts. Heck Reaction. https://chem.libretexts.org/Bookshelves/Inorganic_Chemistry/Supplemental_Modules_and_Websites_(Inorganic_Chemistry)/Catalysis/Catalyst_Examples/Heck_Reaction (accessed 2025-04-30).

  Libretexts. Suzuki-Miyaura Coupling. https://chem.libretexts.org/Bookshelves/Inorganic_Chemistry/Supplemental_Modules_and_Websites_(Inorganic_Chemistry)/Catalysis/Catalyst_Examples/Suzuki-Miyaura_Coupling (accessed 2025-04-30).

  Myers, A. G. The Noyori Asymmetric Hydrogenation Reaction. https://hwpi.harvard.edu/files/myers/files/18-noyori_asymmetric_hydrogenation_reaction.pdf (accessed 2025-04-30).

  Myers, A. G. The Sharpless Asymmetric Epoxidation Reaction. https://hwpi.harvard.edu/files/myers/files/22-sharpless_asymmetric_epoxidation_reaction.pdf (accessed 2025-04-30).

  Nicolaou, K. C.; Yang, Z.; Liu, J. J.; Ueno, H.; Nantermet, P. G.; Guy, R. K.; Claiborne, C. F.; Renaud, J.; Couladouros, E. A.; Paulvannan, K.; Sorensen, E. J. Total Synthesis of Taxol. Nature 1994, 367, 630–634. https://doi.org/10.1038/367630a0.

  de Vries, J. G. The Heck Reaction in the Production of Fine Chemicals. Can. J. Chem. 2001, 79 (5–6), 1086–1092. https://doi.org/10.1139/v01-033.

• SK. Cativa Process for Acetic Acid Synthesis. Chem-Station Int. Ed. May 11, 2017. https://en.chem-station.com/reactions-2/2017/05/cativa-process-for-acetic-acid-synthesis.html
• Haynes, A.; Maitlis, P. M.; Morris, G. E.; Sunley, G. J.; Adams, H.; Badger, P. W.; Bowers, C. M.; Cook, D. B.; Elliott, P. I. P.; Ghaffar, T.; Green, H.; Griffin, T. R.; Payne, M.; Pearson, J. M.; Taylor, M. J.; Vickers, P. W.; Watt, R. J. Promotion of Iridium-Catalyzed Methanol Carbonylation: Mechanistic Studies of the Cativa Process. Catal. Today 2000, 58, 19–32. https://doi.org/10.1016/S0920-5861(00)00263-7:contentReference[oaicite:22]{index=22}
• SK. Monsanto Process for Acetic Acid Synthesis. Chem-Station Int. Ed. May 11, 2017. https://en.chem-station.com/reactions-2/2017/05/monsanto-process-for-acetic-acid-synthesis.html

• Organometallics 2019, 38, 1, 3–35 https://pubs.acs.org/doi/10.1021/acs.organomet.8b00720
• Chemistry Libre Texts, Organometallic Chemsitry. https://chem.libretexts.org/Courses/East_Tennessee_State_University/CHEM_3110%3A_Descriptive_Inorganic_Chemistry/11%3A_Organometallic_Chemistry/11.03%3A_Oxidative_Addition
• https://chem.libretexts.org/Bookshelves/Inorganic_Chemistry/Supplemental_Modules_and_Websites_(Inorganic_Chemistry)/Advanced_Inorganic_Chemistry_(Wikibook)/01%3A_Chapters/1.26%3A_Oxidative_Addition_Reductive_Elimination
• https://chem.libretexts.org/Bookshelves/Inorganic_Chemistry/Introduction_to_Organometallic_Chemistry_(Ghosh_and_Balakrishna)/10%3A_Reaction_Mechanisms/10.01%3A_Oxidative_Addition_and_Reductive_Elimination
• https://alpha.chem.umb.edu/chemistry/ch611/documents/Lec16OxidativeAddition_000.pdf