Crossref Cited-by Linking logo

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. Bulletin of the Chemical Society of Japan 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>
  • Chen Ming, Roush William R.: Enantioselective Synthesis of (+)-Crocacin C. An Example of a Highly Challenging Mismatched Double Asymmetric δ-Stannylcrotylboration Reaction. Org. Lett. 2012, 14, 1880. <https://doi.org/10.1021/ol300476f>
  • Gagnepain Julien, Moulin Emilie, Fürstner Alois: Gram‐Scale Synthesis of Iejimalide B. Chemistry A European 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>
  • Andrade Rodrigo B.: Syntheses of the Crocacins. A Review. Org Preparations & Procedures Int 2009, 41, 359. <https://doi.org/10.1080/00304940903188084>
  • Feutrill John T., Lilly Michael J., White Jonathan M., Rizzacasa Mark A.: Asymmetric total synthesis of the myxobacteria metabolites crocacins A–D. Tetrahedron 2008, 64, 4880. <https://doi.org/10.1016/j.tet.2008.01.139>
  • Sirasani Gopal, Paul Tapas, Andrade Rodrigo B.: Concise Total Synthesis of (+)-Crocacin C. J. Org. Chem. 2008, 73, 6386. <https://doi.org/10.1021/jo800906p>
  • Fürstner Alois, Funel Jacques-Alexis, Tremblay Martin, Bouchez Laure C., Nevado Cristina, Waser Mario, Ackerstaff Jens, Stimson Christopher C.: A versatile protocol for Stille–Migita cross coupling reactions. Chem. Commun. 2008, 2873. <https://doi.org/10.1039/b805299a>
  • Dias Luiz C., de Oliveira Luciana G., Meira Paulo R. R.: Recent results toward the stereoselective synthesis of biologically active natural products. Pure and Applied Chemistry 2007, 79, 163. <https://doi.org/10.1351/pac200779020163>
  • Besev Magnus, Brehm Christof, Fuerstner Alois: Formal Total Syntheses of Crocacin A—D. ChemInform 2006, 37. <https://doi.org/10.1002/chin.200616211>
  • Fürstner Alois, Kattnig Egmont, Lepage Olivier: Total Syntheses of Amphidinolide X and Y. J. Am. Chem. Soc. 2006, 128, 9194. <https://doi.org/10.1021/ja061918e>