@article{0650f851a919461c972a0761f3d0d294,
title = "Synthesis of dysiherbaine analogue",
abstract = "Synthesis of dysiherbaine analogue 4, which corresponds to 8,9-epi-neodysiherbaine A, is described. The synthesis features a concise route to the bicyclic ether skeleton through stereoselective C-glycosylation to set the C6 stereocenter and 5-exo ring-closure to form the tetrahydrofuran ring. The results of preliminary biological studies of 4 are also provided.",
author = "Muneo Shoji and Kaoru Shiohara and Masato Oikawa and Ryuichi Sakai and Makoto Sasaki",
note = "Funding Information: This work was financially supported by Yamada Science Foundation and a Grant-in-Aid for Scientific Research on Priority Area {\textquoteleft}Creation of Biologically Functional Molecules{\textquoteright} from the Ministry of Education, Science, Sports, Culture and Technology, Japan.",
year = "2005",
month = aug,
day = "15",
doi = "10.1016/j.tetlet.2005.06.093",
language = "English",
volume = "46",
pages = "5559--5562",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Ltd.",
number = "33",
}