Literature DB >> 27295068

An efficient method for the synthesis of pyranoid glycals.

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.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Acetonitrile; Ammonium chloride; Glycals; Glycopyranosyl bromides; Zinc

Mesh:

Substances:

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


  2 in total

1.  P(v) intermediate-mediated E1cB elimination for the synthesis of glycals.

Authors:  Fen Liu; Haiyang Huang; Longgen Sun; Zeen Yan; Xiao Tan; Jing Li; Xinyue Luo; Haixin Ding; Qiang Xiao
Journal:  Chem Sci       Date:  2022-04-22       Impact factor: 9.969

2.  TMSOTf mediated stereoselective synthesis of α-C-glycosides from unactivated aryl acetylenes.

Authors:  Heshan Chen; Xiaosheng Luo; Saifeng Qiu; Wengjie Sun; Jianbo Zhang
Journal:  Glycoconj J       Date:  2016-08-26       Impact factor: 2.916

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.