| Literature DB >> 27295068 |
Heshan Chen1, Ting Xian1, Wan Zhang1, Wenshuai Si1, Xiaosheng Luo1, Bo Zhang1, Meiyu Zhang1, Zhongfu Wang2, Jianbo Zhang3.
Abstract
A simple and efficient procedure was designed for the preparation of pyranoid glycals. In a novel fashion, a series of protected glycopyranosyl bromides underwent reductive elimination in the presence of zinc dust and ammonium chloride in CH3CN at 30-60 °C. The corresponding glycals were obtained with excellent isolated yields (72-96%) in a short time (20-50 min). Furthermore, the transformation was compatible with different protection patterns and conveniently scalable (86% for 45 g acetobromoglucose) which made it very applicable in organic synthesis.Entities:
Keywords: Acetonitrile; Ammonium chloride; Glycals; Glycopyranosyl bromides; Zinc
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Year: 2016 PMID: 27295068 DOI: 10.1016/j.carres.2016.05.013
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104