Digital Library
Close Browse articles from a journal
 
<< previous    next >>
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
           All articles of the corresponding issues
                                       Details for article 91 of 116 found articles
 
 
  Synthesis of Glycoside Derivatives Employing the Ferrier Rearrangement
 
 
Title: Synthesis of Glycoside Derivatives Employing the Ferrier Rearrangement
Author: Wieczorek, Eusebius
Thiem, Joachim
Appeared in: Journal of carbohydrate chemistry
Paging: Volume 17 (1998) nr. 4-5 pages 785-809
Year: 1998-05-01
Contents: Various glycals underwent smooth Lewis acid-catalysed allylic rearrangement reactions with O-nucleophiles to yield 2,3-unsaturated glycoside derivatives. In the hexose series predominantly α-D-, and in the pentose series β-D-anomers resulted. Among others Ω-cyano- as well as Ω-benzyloxycarbonylamino functionalised alcohols could be used successfully. With diols the corresponding 1,1'-bridged disaccharides could be obtained.
Publisher: Taylor & Francis
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 91 of 116 found articles
 
<< previous    next >>
 
 Koninklijke Bibliotheek - National Library of the Netherlands