- 1) Ohno, S., Tomita-Yokotani, K., Kosemura, S., Node, M., Suzuki, T., Amano, M., Yasui, K., Goto, T., Yamamura, S., and Hasegawa, K., A species-selective allelopathic substance from germinating sunflower (Helianthus annuus L.) seeds. Phytochemistry, 56, 577–581 (2001).
- 2) Kuo, Y.-H., and Lin, B.-Y., A new dinorxanthane and chromone from the root of Tithonia diversifolia. Chem. Pharm. Bull., 47, 428–429 (1999).
- 3) Yokoe, H., Sasaki, H., Yoshimura, T., Shindo, M., Yoshida, M., and Shishido, K., Total synthesis of (+)-sundiversifolide. Org. Lett., 9, 969–971 (2007).
- 4) Takikawa, H., Tobe, M., and Sasaki, M., Synthesis and absolute configuration of annuionone A. Tetrahedron, 61, 8830–8835 (2005).
- 5) Takikawa, H., Imamura, Y., and Sasaki, M., Synthesis and absolute configuration of brevione B, an allelochemical isolated from Penicillium sp. Tetrahedron, 62, 39–48 (2006).
- 6) Takikawa, H., Synthetic studies on allelopathic terpenoids. Yuki Gosei Kagaku Kyokaishi (in Japanese), 64, 819–826 (2006).
- 7) Snider, B. B., and Patricia, J. J., Manganese(III)-based oxidative free-radical cyclizations. Oxidative cyclization and aromatization of 3-oxo-6-heptenoate esters. J. Org. Chem., 54, 38–46 (1989).
- 8) Marshall, J. A., and Litsas, S. B., Reduction of α-substituted acetoacetate enolates with lithium aluminum hydride. J. Org. Chem., 37, 1840–1842 (1972).
- 9) Soai, K., Chemoselective reductions with sodium borohydride and lithium borohydride in mixed solvents. Yuki Gosei Kagaku Kyokaishi (in Japanese), 45, 1148–1156 (1987).
- 10) Soai, K., and Oyamada, H., A chemoselective one-pot reduction of β-ketoesters to 1,3-diols. Synthesis, 605–607 (1984).
- 11) Comin, M. J., Parrish, D. A., Deschamps, J. F., and Marquez, V. E., Synthesis of bicyclo[3.1.0]hexanes functionalized at the tip of the cyclopropane ring. Application to the synthesis of carbocyclic nucleosides. Org. Lett., 8, 705–708 (2006).
- 12) Mori, I., Takai, K., Oshima, K., and Nozaki, H., Organoaluminium assisted rearrangements of five-membered ring enol ethers with vinyl substituents. Tetrahedron, 40, 4013–4018 (1984).
- 13) Sisu, E., Sollogoub, M., Mallet, J.-M., and Sinaÿ, P., Cycloheptanic sugar mimetics, bridging the gap in the homologous series of carbocyclic analogues. Tetrahedron, 58, 10189–10196 (2002).
- 14) Jia, C., Zhang, Y., and Zhang, L., High stereoselective synthesis of a seven-membered carbasugar via triisobutylaluminium promoted Claisen rearrangement. Tetrahedron: Asymmetry, 14, 2195–2199 (2003).
Bioscience, Biotechnology, and Biochemistry
Volume 71, 2007 - Issue 8