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Pure Appl. Chem., 1994, Vol. 66, No. 10-11, pp. 2071-2074

http://dx.doi.org/10.1351/pac199466102071

Application of the aza-Claisen rearrangement to the total synthesis of natural products: (-)-Isoiridomyrmecin

S. Itô and T. Tsunoda

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  • Duhamel Nina, Rye Claire E., Barker David: Total Synthesis of ent -Hyperione A and ent -Hyperione B. Asian Journal of Organic Chemistry 2013, 2, 491. <http://dx.doi.org/10.1002/ajoc.201300086>
  • Majumdar K.C., Nandi Raj Kumar: The Claisen rearrangement in the syntheses of bioactive natural products. Tetrahedron 2013, 69, 6921. <http://dx.doi.org/10.1016/j.tet.2013.06.003>
  • Ishihara Jun, Watanabe Yuki, Koyama Noriko, Nishino Yukihiro, Takahashi Keisuke, Hatakeyama Susumi: Indium-mediated Reformatsky–Claisen rearrangement. Tetrahedron 2011, 67, 3659. <http://dx.doi.org/10.1016/j.tet.2011.03.079>
  • Takeda Kazutaka, Toyota Masahiro: Scope and applications of second generation palladium-catalyzed cycloalkenylation. Stereoselective total syntheses of isoiridomyrmecin, isodihydronepetalactone, and α-skytanthine. Tedrahedron 2011, 67, 9909. <http://dx.doi.org/10.1016/j.tet.2011.08.078>
  • Rye Claire E., Barker David: Asymmetric Synthesis of (+)-Galbelgin, (−)-Kadangustin J, (−)-Cyclogalgravin and (−)-Pycnanthulignenes A and B, Three Structurally Distinct Lignan Classes, Using a Common Chiral Precursor. J Org Chern 2011, 76, 6636. <http://dx.doi.org/10.1021/jo200968f>
  • ITO S., TSUNODA T.: ChemInform Abstract: Application of the Aza-Claisen Rearrangement to the Total Synthesis of Natural Products: (-)-Isoiridomyrmecin. ChemInform 2010, 26, no. <http://dx.doi.org/10.1002/chin.199507294>
  • Davies Stephen G., Garner A. Christopher, Nicholson Rebecca L., Osborne James, Roberts Paul M., Savory Edward D., Smith Andrew D., Thomson James E.: Doubly diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements. Org Biomol Chem 2009, 7, 2604. <http://dx.doi.org/10.1039/b902753j>
  • ITÔ Shô: Development of New Synthetic Reagents in Mitsunobu-Type Reaction. YAKUGAKU ZASSHI 2001, 121, 567. <http://dx.doi.org/10.1248/yakushi.121.567>
  • Grayson David H.: Monoterpenoids. Nat Prod Rep 1997, 14, 477. <http://dx.doi.org/10.1039/np9971400477>
  • Tsunoda Tetsuto, Yamamoto Hidetoshi, Goda Kayo, Itô Shô: Mitsunobu-type alkylation of p-toluenesulfonamide. A convenient new route to primary and secondary amines. Tetrahetron Lett 1996, 37, 2457. <http://dx.doi.org/10.1016/0040-4039(96)00317-6>
  • Tsunoda Tetsuto, Ozaki Fumie, Shirakata Nozomi, Tamaoka Yuki, Yamamoto Hidetoshi, Itô Shô: Formation of heterocycles by the Mitsunobu reaction. Stereoselective synthesis of (+)-α-skytanthine. Tetrahetron Lett 1996, 37, 2463. <http://dx.doi.org/10.1016/0040-4039(96)00319-X>
  • Enders Dieter, Knopp Monika, Schiffers Robert: Asymmetric [3.3]-sigmatropic rearrangements in organic synthesis. Tet Asymm 1996, 7, 1847. <http://dx.doi.org/10.1016/0957-4166(96)00220-0>
  • Tsunoda Tetsuto, Nagaku Miwa, Nagino Chisato, Kawamura Yumi, Ozaki Fumie, Hioki Hideaki, Itô Shô: Carbon-carbon bond formation with new Mitsunobu reagents. Tetrahetron Lett 1995, 36, 2531. <http://dx.doi.org/10.1016/0040-4039(95)00300-2>