English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
 
 
DownloadE-Mail
  O-glycoside synthesis with glycosyl iodides under neutral conditions in 1 M LiClO4 in CH2Cl2

Schmid, U., & Waldmann, H. (1997). O-glycoside synthesis with glycosyl iodides under neutral conditions in 1 M LiClO4 in CH2Cl2. LIEBIGS ANNALEN-RECUEIL, (12), 2573-2577.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Schmid, U1, Author
Waldmann, Herbert2, Author           
Affiliations:
1external, ou_persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

Content

show
hide
Free keywords: glycosides; glycosylations; glycosyl iodides; glycosyl phosphates; LiClO4; solvent mixtures;
 Abstract: Glycosyl phosphates, imidates, trifluoroacetates, chlorides, and bromides are converted into the respective glycosyl iodides by treatment with LiI or NaI in 1 M solutions of LiClO4 in CH2Cl2. Under these neutral conditions the reactive glycosyl iodides are activated, and react with different glycosyl acceptors to give O-glycosides in moderate yields, with the alpha-anomers predominating. The glycosylation reactions most probably proceed by the initial formation of beta-configured glycosyl iodides from the alpha-configured precursors, and subsequent attack of the glycosyl acceptor on the equatorial iodide from the axial direction.

Details

show
hide
Language(s): eng - English
 Dates: 1997-12
 Publication Status: Issued
 Pages: 5
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000071041900022
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: LIEBIGS ANNALEN-RECUEIL
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Weinheim : VCH
Pages: - Volume / Issue: (12) Sequence Number: - Start / End Page: 2573 - 2577 Identifier: ISSN: 0947-3440