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- Convenient synthesis of (+)-valiolamine and (−)-1-epi-valiolamine from (−)-vibo-quercitol. Seiichiro Ogawa, Yo Ohishi, Miwako Asada, Akihiro Tomoda, Atsushi Takahashi, Yoriko Ooki, Midori Mori, Masayoshi Itoh, Takashi Korenaga
, Org. Biomol. Chem.
, 2004
, 2
, 884
- The C7N aminocyclitol family of natural products. Taifo Mahmud
, Nat. Prod. Rep.
, 2003
, 20
, 137
- Synthesis and trehalase-inhibitory activity of an imino-linked dicarba-α,α-trehalose and analogues thereof. Seiichiro Ogawa, Koji Sato, Yasunobu Miyamoto
, J. Chem. Soc., Perkin Trans. 1
, 1993
, 691
- Synthesis and biological activity of naturally occurring α-glucosidase inhibitors. Duncan J. Wardrop, Samanthi L. Waidyarachchi
, Nat. Prod. Rep.
, 2010
, 27
, 1431
- Recent applications of olefin metathesis and related
reactions in carbohydrate chemistry. René Roy, Sanjoy Kumar Das
, Chem. Commun.
, 2000
, 519
- Synthetic applications of hypophosphite derivatives in reduction. Carole Guyon, Estelle Métay, Florence Popowycz, Marc Lemaire
, Org. Biomol. Chem.
, 2015
, 13
, 7879
- Intramolecular direct aldol reactions of sugar 2,7-diketones: syntheses of hydroxylated cycloalka(e)nones. Tony K. M. Shing, Hau M. Cheng
, Org. Biomol. Chem.
, 2015
, 13
, 4795
- Natural products from plants targeting key enzymes for the future development of antidiabetic agents. R. Mata, L. Flores-Bocanegra, B. Ovalle-Magallanes, M. Figueroa
, Nat. Prod. Rep.
, 2023
, 40
, 1198
- Divergent synthesis of new α-glucosidase inhibitors obtained through a vinyl Grignard-mediated carbocyclisation. Ida M. B. Knudsen, Christinne Hedberg, Lucy Kate Ladefoged, Daisuke Ide, Anne Brinkø, Espen Z. Eikeland, Atsushi Kato, Henrik H. Jensen
, Org. Biomol. Chem.
, 2018
, 16
, 6250
- The conformational rigidity of butane-1,2-diacetals as a powerful synthetic tool. Emilio Lence, Luis Castedo, Concepción González-Bello
, Chem. Soc. Rev.
, 2008
, 37
, 1689