@article{73a500a168b94744bd02b7271fdc2c4a,
title = "Synthetic Route to 2-Deoxyaldoses by Fluoride-Catalyzed Solvolysis of Enol-Phosphate Esters",
abstract = "1-Alkenyl and phenyl phosphate esters undergo smooth cleavage of the phosphorus-oxygen linkage by fluoride-catalyzed alcoholysis to give aldehydes (ketones) and phenols, respectively. Application of this method provides a new route to 2-deoxyaldosugars from the enol-phosphates derived from vinylene carbonate telomers.",
keywords = "2-deoxyaldose, aryl phosphate, cesium fluoride, enol phosphate, vinylene carbonate telomer",
author = "Naoki Mitsuo and Yoshihiro Abe and Takeo Takizawa and Takehisa Kunieda",
note = "Copyright: Copyright 2017 Elsevier B.V., All rights reserved.",
year = "1980",
doi = "10.1248/cpb.28.1327",
language = "English",
volume = "28",
pages = "1327--1330",
journal = "Chemical and Pharmaceutical Bulletin",
issn = "0009-2363",
publisher = "Pharmaceutical Society of Japan",
number = "4",
}