Alternaric acid: formal synthesis and related studies

Scholarly Works

• Agbaria, M.; Egbaria, N.; Nairoukh, Z. Unveiling Novel Synthetic Pathways through Brook Rearrangement. Synthesis 2024. doi:10.1055/a-2257-7304
• Kaur, N. Six-membered O-heterocycles. Iodine-Assisted Synthesis of Six- and Seven-Membered Heterocycles; Elsevier, 2023; pp 175–199. doi:10.1016/b978-0-443-15225-2.00010-4
• Moriyama, M.; Liu, X.; Enoki, Y.; Matsumoto, K.; Tanabe, Y. Asymmetric Total Syntheses of Both Enantiomers of Plymuthipyranone B and Its Unnatural Analogues: Evaluation of anti-MRSA Activity and Its Chiral Discrimination. Pharmaceuticals (Basel, Switzerland) 2021, 14, 938. doi:10.3390/ph14090938
• Shan, C.; Zhong, K.; Qi, X.; Xu, D.; Qu, L.; Bai, R.; Lan, Y. Long distance unconjugated agostic-assisted 1,5-H shift in a Ru-mediated Alder-ene type reaction: mechanism and stereoselectivity. Organic Chemistry Frontiers 2018, 5, 3178–3185. doi:10.1039/c8qo00699g
• Blakemore, P. R.; Sephton, S. M.; Ciganek, E. Organic Reactions; Wiley, 2018; pp 1–261. doi:10.1002/0471264180.or095.01
• Merchant, R. R.; Edwards, J. T.; Qin, T.; Kruszyk, M. M.; Bi, C.; Che, G.; Bao, D. H.; Qiao, W.; Sun, L.; Collins, M. R.; Fadeyi, O. O.; Gallego, G. M.; Mousseau, J. J.; Nuhant, P.; Baran, P. S. Modular radical cross-coupling with sulfones enables access to sp3-rich (fluoro)alkylated scaffolds. Science (New York, N.Y.) 2018, 360, 75–80. doi:10.1126/science.aar7335
• Haimov, E.; Nairoukh, Z.; Shterenberg, A.; Berkovitz, T.; Jamison, T. F.; Marek, I. Stereoselective Formation of Fully Substituted Ketone Enolates. Angewandte Chemie 2016, 128, 5607–5610. doi:10.1002/ange.201601883
• Haimov, E.; Nairoukh, Z.; Shterenberg, A.; Berkovitz, T.; Jamison, T. F.; Marek, I. Stereoselective Formation of Fully Substituted Ketone Enolates. Angewandte Chemie (International ed. in English) 2016, 55, 5517–5520. doi:10.1002/anie.201601883
• Lin, C.-Y.; Ma, P.-J.; Sun, Z.; Lu, C.-D.; Xu, Y.-J. Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides. Chemical communications (Cambridge, England) 2016, 52, 912–915. doi:10.1039/c5cc08118a
• Tan, C.; Chen, W.; Mu, X.; Chen, Q.; Gong, J.; Luo, T.; Yang, Z. Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I. Organic letters 2015, 17, 2338–2341. doi:10.1021/acs.orglett.5b00831
• Shi, H.; Tan, C.; Zhang, W.; Zhang, Z.; Long, R.; Luo, T.; Yang, Z. Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I. Organic letters 2015, 17, 2342–2345. doi:10.1021/acs.orglett.5b00829
• Eppe, G.; Didier, D.; Marek, I. Stereocontrolled Formation of Several Carbon–Carbon Bonds in Acyclic Systems. Chemical reviews 2015, 115, 9175–9206. doi:10.1021/cr500715t
• Kk, K.; A, G. Male Hypothyroidism-Clinical Relevance Including Role in Reproduction. Journal of Diabetes, Metabolic Disorders & Control 2015, 2. doi:10.15406/jdmdc.2015.02.00029
• Jin, R.; Liu, S.; Lan, Y. Distortion–interaction analysis along the reaction pathway to reveal the reactivity of the Alder-ene reaction of enes. RSC Advances 2015, 5, 61426–61435. doi:10.1039/c5ra10345b
• Corbett, M. T.; Johnson, J. S. Dynamic Kinetic Asymmetric Transformations of β-Stereogenic α-Ketoesters by Direct Aldolization†. Angewandte Chemie (International ed. in English) 2013, 53, 255–259. doi:10.1002/anie.201306873
• Corbett, M. T.; Johnson, J. S. Dynamic Kinetic Asymmetric Transformations of β‐Stereogenic α‐Ketoesters by Direct Aldolization. Angewandte Chemie 2013, 126, 259–263. doi:10.1002/ange.201306873

Explore citations to this article at