﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Research Letters in Organic Chemistry</title><link>http://www.hindawi.com</link><description>The latest articles from Hindawi Publishing Corporation</description><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright><item><title>Syntheses of 5-Thio-D-Mannose from Petrochemicals and a Disaccharide Analog Containing It</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/784173</link><description>Per-O-acetyl-5-thio-DL-mannose was synthesized from petrochemicals in six steps and 9&amp;#37; overall yield. It was then derivatized into glycosyl trichloroacetimidate and subjected to glycosidation reaction with a mannosyl acceptor to give a separatable mixture of disaccharides with 5-thio-D- and L-mannosides. This is the first synthesis of an enantiomerically pure 5-thiosugar derivative from racemic chemicals. The D-glycoside was derivatized into methyl (5-thio-&amp;#x03B1;-D-mannopyranosyl)-2-O-&amp;#x03B1;-D-mannopyranoside 6-phosphate as a potential inhibitor of a golgi &amp;#x03B1;-1,2-mannosidase.</description><Author>Hideya Yuasa, Masatake Jouyabu, Nobuyuki Mitsuhashi, and Hironobu Hashimoto</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item></channel></rss>