English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Synthesis of 2-deoxy and 2,6-dideoxy glycosides under neutral conditions in LiClO4/Et2O mixtures

Schene, H., & Waldmann, H. (1998). Synthesis of 2-deoxy and 2,6-dideoxy glycosides under neutral conditions in LiClO4/Et2O mixtures. CHEMICAL COMMUNICATIONS, (24), 2759-2760. doi:10.1039/a807734g.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Schene, H1, 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: HIGHLY STEREOSELECTIVE GLYCOSYLATION; DIELS-ALDER REACTIONS; ORGANIC-SOLVENTS; CONCENTRATED-SOLUTIONS; 2-DEOXY-BETA-GLYCOSIDIC LINKAGES; DONORS; CONSTRUCTION; ANTHRACYCLINES; FLUORIDES; GLYCALS
 Abstract: Glycosides of 2-deoxy and 2,6-dideoxy carbohydrates were built up in high yields and with high stereoselectivity in 0.1 M LiClO4/Et2O mixtures; the glycosidations proceed under neutral conditions and without need for an additional promoter such as a strong Lewis acid, a heavy metal salt or an alkylating reagent.

Details

show
hide
Language(s): eng - English
 Dates: 1998
 Publication Status: Published in print
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000077611400043
DOI: 10.1039/a807734g
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: CHEMICAL COMMUNICATIONS
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: CAMBRIDGE UK : ROYAL SOC CHEMISTRY
Pages: - Volume / Issue: (24) Sequence Number: - Start / End Page: 2759 - 2760 Identifier: ISSN: 1359-7345