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Collect. Czech. Chem. Commun. 2005, 70, 1696-1708
https://doi.org/10.1135/cccc20051696

Formal Total Syntheses of Crocacin A-D

Magnus Besev, Christof Brehm and Alois Fürstner*

Max-Planck-Institut für Kohlenforschung, D-45470 Mülheim/Ruhr, Germany

Crossref Cited-by Linking

  • Kumaraswamy Gullapalli, Narayanarao Vykunthapu, Shanigaram Prakash, Balakishan Guniganti: Diastereoselective synthesis of an advanced intermediate of the crocacin family using asymmetric transfer hydrogenation-DKR and Marshall allenylation as key reactions. Tetrahedron 2015, 71, 8960. <https://doi.org/10.1016/j.tet.2015.09.057>
  • Infante-Rodriguez Carolina, Domon Lisianne, Breuilles Pascal, Uguen Daniel: Asymmetric Synthesis of Stigmatellin and Crocacin C. BCSJ 2015, 88, 308. <https://doi.org/10.1246/bcsj.20140271>
  • Pasqua Adele E., Ferrari Frank D., Crawford James J., Marquez Rodolfo, Li Xiao-Juan, Xiong Heng-Ying, Hua Ming-Qing, Nie Jing, Zheng Yan, Ma Jun-An: Formal synthesis of (+)-crocacin C. Tetrahedron Letters 2012, 53, 2114. <https://doi.org/10.1016/j.tetlet.2012.02.049>
  • Pasqua Adele E., Ferrari Frank D., Hamman Chris, Liu Yanzhou, Crawford James J., Marquez Rodolfo: Step-Economic Synthesis of (+)-Crocacin C: A Concise Crotylboronation/[3,3]-Sigmatropic Rearrangement Approach. J. Org. Chem. 2012, 77, 6989. <https://doi.org/10.1021/jo301210f>
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  • Gagnepain Julien, Moulin Emilie, Fürstner Alois: Gram-Scale Synthesis of Iejimalide B. Chem Eur J 2011, 17, 6964. <https://doi.org/10.1002/chem.201100178>
  • Moulin Emilie, Nevado Cristina, Gagnepain Julien, Kelter Gerhard, Fiebig Heinz-Herbert, Fürstner Alois: Synthesis and evaluation of an Iejimalide-archazolid chimera. Tetrahedron 2010, 66, 6421. <https://doi.org/10.1016/j.tet.2010.05.043>
  • Candy Mathieu, Audran Gérard, Bienaymé Hugues, Bressy Cyril, Pons Jean-Marc: Total Synthesis of (+)-Crocacin C Using Hidden Symmetry. J. Org. Chem. 2010, 75, 1354. <https://doi.org/10.1021/jo902582w>
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