@article{11f8a13328a84377a53c56cc364d4399,
title = "Stereoselective synthesis of scyphostatin hydrophilic moiety",
abstract = "A stereoselective synthesis of scyphostatin hydrophilic moiety was accomplished. Substrate- and reagent-controlled dihydroxylation of tri- and monosubstituted alkenes afforded desired diols, respectively. Chemo- and stereoselective allylation of α-(methoxycarbonyl)cyclohexanone provided allylcyclohexanol. Oxidative cleavage of glycol and subsequent β-elimination of siloxycyclohexanone furnished the desired epoxycyclohexenone.",
keywords = "Epoxycyclohexenone, Hydrophilic moiety, Scyphostatin, Stereoselective allylation, Stereoselective dihydroxylation",
author = "Kazuaki Kuwata and Masashi Suzuki and Yoshikazu Inami and Kengo Hanaya and Takeshi Sugai and Mitsuru Shoji",
note = "Funding Information: This work was supported by MEXT -Supported Program for the Strategic Research Foundation at Private Universities, 2011–2015. ",
year = "2014",
month = apr,
day = "23",
doi = "10.1016/j.tetlet.2014.03.077",
language = "English",
volume = "55",
pages = "2856--2858",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "17",
}