User:Sganz3/Choose an Article

Article Selection
Please list articles that you're considering for your Wikipedia assignment below. Begin to critique these articles and find relevant sources.

Option 1

 * Amide Reduction
 * Stub
 * (add more reactions to make this happen!)
 * Not many sources.
 * Sources:
 * (1) Alcântara, Antônio Flávio de Carvalho, Hiléia dos Santos Barroso, and Dorila Piló-Veloso. “Redução de Amidas Por Boranos.” Química Nova 25, no. 2 (May 2002): 300–311. https://doi.org/10.1590/S0100-40422002000200018. (2) Chardon, A.; Morisset, E.; Rouden, J.; Blanchet, J. Recent Advances in Amide Reductions. Synthesis 2018, 50 (05), 984–997. https://doi.org/10.1055/s-0036-1589144 . (3) Khalimon, A.; Gudun, K.; Hayrapetyan, D. Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines. Catalysts 2019, 9 (6), 490. https://doi.org/10.3390/catal9060490.
 * Sources:
 * (1) Alcântara, Antônio Flávio de Carvalho, Hiléia dos Santos Barroso, and Dorila Piló-Veloso. “Redução de Amidas Por Boranos.” Química Nova 25, no. 2 (May 2002): 300–311. https://doi.org/10.1590/S0100-40422002000200018. (2) Chardon, A.; Morisset, E.; Rouden, J.; Blanchet, J. Recent Advances in Amide Reductions. Synthesis 2018, 50 (05), 984–997. https://doi.org/10.1055/s-0036-1589144 . (3) Khalimon, A.; Gudun, K.; Hayrapetyan, D. Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines. Catalysts 2019, 9 (6), 490. https://doi.org/10.3390/catal9060490.

Option 2

 * Amide (functional group)
 * Stub
 * Not much information about potential reactions, history of this group, etc, when it is very significant.
 * Sources:
 * (1) Amide - an overview | ScienceDirect Topics. https://www.sciencedirect.com/topics/chemical-engineering/amide (accessed 2022-10-02). (2)  Li, G.; Ma, S.; Szostak, M. Amide Bond Activation: The Power of Resonance. Trends in Chemistry 2020, 2 (10), 914–928. https://doi.org/10.1016/j.trechm.2020.08.001.
 * Sources:
 * (1) Amide - an overview | ScienceDirect Topics. https://www.sciencedirect.com/topics/chemical-engineering/amide (accessed 2022-10-02). (2)  Li, G.; Ma, S.; Szostak, M. Amide Bond Activation: The Power of Resonance. Trends in Chemistry 2020, 2 (10), 914–928. https://doi.org/10.1016/j.trechm.2020.08.001.

Option 3

 * Cycloalkene
 * Stub
 * Almost nothing about what reactions you can do with this, or about how to synthesize it.
 * Sources:
 * (1) Ito, T.; Tsutsumi, M.; Yamada, K.; Takikawa, H.; Yamaoka, Y.; Takasu, K. Synthesis of Functionalized Medium‐Sized Trans ‐Cycloalkenes by 4π Electrocyclic Ring Opening/Alkylation Sequence. Angew. Chem. Int. Ed. 2019, 58 (34), 11836–11840. https://doi.org/10.1002/anie.201906665 . (2)  Zhang, J.; Niu, Y.; Cao, X.; Ye, X.-S. Convenient One-Pot Synthesis of Thiosugars and Their Efficient Conversion to Polyoxygenated Cycloalkenes. Tetrahedron 2012, 68 (22), 4242–4247. https://doi.org/10.1016/j.tet.2012.03.086 .  (3)  Jackson, S. D.; Kelly, G. J.; Watson, S. R.; Gulickx, R. Cycloalkene Hydrogenation over Palladium Catalysts. Applied Catalysis A: General 1999, 187 (1), 161–168. https://doi.org/10.1016/S0926-860X(99)00204-5.
 * Sources:
 * (1) Ito, T.; Tsutsumi, M.; Yamada, K.; Takikawa, H.; Yamaoka, Y.; Takasu, K. Synthesis of Functionalized Medium‐Sized Trans ‐Cycloalkenes by 4π Electrocyclic Ring Opening/Alkylation Sequence. Angew. Chem. Int. Ed. 2019, 58 (34), 11836–11840. https://doi.org/10.1002/anie.201906665 . (2)  Zhang, J.; Niu, Y.; Cao, X.; Ye, X.-S. Convenient One-Pot Synthesis of Thiosugars and Their Efficient Conversion to Polyoxygenated Cycloalkenes. Tetrahedron 2012, 68 (22), 4242–4247. https://doi.org/10.1016/j.tet.2012.03.086 .  (3)  Jackson, S. D.; Kelly, G. J.; Watson, S. R.; Gulickx, R. Cycloalkene Hydrogenation over Palladium Catalysts. Applied Catalysis A: General 1999, 187 (1), 161–168. https://doi.org/10.1016/S0926-860X(99)00204-5.