Nickel‐Catalyzed Arylation, Alkenylation, and Alkynylation of Unprotected Thioglycosides at Room Temperature. Issue 45 (24th September 2013)
- Record Type:
- Journal Article
- Title:
- Nickel‐Catalyzed Arylation, Alkenylation, and Alkynylation of Unprotected Thioglycosides at Room Temperature. Issue 45 (24th September 2013)
- Main Title:
- Nickel‐Catalyzed Arylation, Alkenylation, and Alkynylation of Unprotected Thioglycosides at Room Temperature
- Authors:
- Brachet, Etienne
Brion, Jean‐Daniel
Alami, Mouad
Messaoudi, Samir - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Unprotected thioglycosides were effective nucleophiles for Ni<sup>0</sup>‐catalyzed CS bond‐forming reaction with functionalized (hetero)aryl, alkenyl, and alkynyl halides. The functional‐group tolerance on the electrophilic partner was typically high and the anomeric selectivities of the thioglycosides were high in all cases. The efficiency of this general procedure was well‐demonstrated by the synthesis of 4‐methyl‐7‐thioumbelliferyl‐β‐<sc>D</sc>‐cellobioside (MUS‐CB).</p> </abstract>
- Is Part Of:
- Chemistry. Volume 19:Issue 45(2013)
- Journal:
- Chemistry
- Issue:
- Volume 19:Issue 45(2013)
- Issue Display:
- Volume 19, Issue 45 (2013)
- Year:
- 2013
- Volume:
- 19
- Issue:
- 45
- Issue Sort Value:
- 2013-0019-0045-0000
- Page Start:
- 15276
- Page End:
- 15280
- Publication Date:
- 2013-09-24
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201302999 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3161.xml